Oxazine-based fluorophore compounds for neurospecific imaging

Abstract

The present invention relates to novel oxazine-based fluorophore compounds useful for in vivo neuroimaging, as well as compositions comprising and methods for the use of said compounds. TIFF2023511405000073.tif101154

Description

[Technical Field]

[0001] STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT This invention was made with government support under grant R01EB021362 awarded by the National Institutes of Health. The government has certain rights in the invention.

[0002] Field of Disclosure The present invention relates to novel oxazine-based fluorophore compounds useful for in vivo neuroimaging, as well as compositions comprising and methods for the use of said compounds. [Background technology]

[0003] Background of the Invention More than 300 million surgeries are performed worldwide each year. Despite many recent advances in the treatment of cancer and other diseases, surgery remains the most effective treatment option for many diseases and injuries. The ultimate goal of surgery is to remove or repair tissue while minimizing comorbidities by preserving vital structures such as nerves and blood vessels. Recent technological advances, including minimally invasive robotic-assisted laparoscopic surgery, have improved outcomes and enabled the reliable performance of challenging procedures with minimal risk. Furthermore, preoperative three-dimensional imaging techniques, such as magnetic resonance imaging (MRI) and computed tomography (CT), have significantly improved diagnostic accuracy, staging, and preoperative planning.

[0004] Despite advances, identifying critical structures (e.g., nerves) to preserve or tissues (e.g., tumors) to completely resect during surgery remains challenging. Due to variability in patient anatomy and the limited ability to directly visualize nerves in the surgical field, nerve identification and preservation can be challenging during surgery. Currently, intraoperative nerve detection is performed using a combination of visual inspection, palpation, and electromyographic monitoring. Several imaging modalities, including ultrasound, optical coherence tomography, and confocal endoscopy, have been utilized in clinical studies for nerve detection. However, these lack specificity, resolution, and wide-field imaging capabilities, making it difficult to identify nerve tissue in real time. As a result, nerve injury continues to compromise surgical outcomes. Iatrogenic nerve injury affects up to 63 million patients worldwide each year, causing acute and chronic pain and impaired or lost motor and sensory function. Radical prostatectomy (RP), a surgical procedure involving the removal of the entire prostate gland as a treatment for prostate cancer, is particularly plagued by nerve injury. Furthermore, while minimally invasive techniques such as robotic-assisted RP can achieve cancer control equivalent to open RP while resulting in less blood loss, lower transfusion rates, and faster recovery, these advances do not confer any advantage in nerve-sparing outcomes and actually eliminate the ability to directly palpate tissue.

[0005] A contrast-enhanced diagnostic technique that allows wide-field, real-time identification of neural tissue during surgery would be of great help to surgeons in nerve preservation and would reduce the rate of iatrogenic nerve injury, improving patients' quality of life after surgery.

[0006] Currently, no NIR neurospecific fluorophores exist, and further development of fluorophores is required to obtain suitable candidates for clinical application.Several classes of neurospecific fluorophores have been investigated for FGS. For example, see Gibbs-Strauss et al. Molecular imaging 10, 91-101 (2011) (Non-Patent Document 1); Wu et al. Journal of medicinal chemistry 51, 6682-6688 (2008) (Non-Patent Document 2); Wang et al. The journal of histochemistry and cytochemistry: official journal of the Histochemistry Society 58, 611-621 (2010) (Non-Patent Document 3); Gibbs et al. PloS one 8, e73493 (2013) (Non-Patent Document 4); Stankoff et al. Proceedings of the National Academy of Sciences of the United States of America 103, 9304-9309 (2006) (Non-Patent Document 5); Cotero et al. Molecular imaging and biology: MIB: the official publication of the Academy of Molecular Imaging 14, 708-717 (2012) (Non-patent document 6); Cotero et al. PloS one 10, e0130276 (2015) (Non-patent document 7); Bajaj et al. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 61, 19-30 (2013) (Non-patent document 8); Gibbs-Strauss et al. Molecular imaging 9, 128-140 (2010) (non-patent document 9); Meyers et al.See The Journal of neuroscience: the official journal of the Society for Neuroscience 23, 4054-4065 (2003) (Non-Patent Document 10); Wang et al. The Journal of Neuroscience: the official journal of the Society for Neuroscience 31, 2382-2390 (2011) (Non-Patent Document 11); and Park et al. Theranostics 4, 823-833 (2014) (Non-Patent Document 12). Of these, oxazine 4 is the most promising candidate for development, exhibiting high neurospecificity and red-shifted absorption and emission spectra close to the NIR (Park et al. Theranostics 4, 823-833 (2014) (Non-Patent Document 12)).

[0007] While useful oxazine nerve-sparing fluorophores are disclosed in International Application PCT / US2019 / 045347, there remains a need for such compounds, particularly for use in aqueous compositions. [Prior art documents] [Patent documents]

[0008] [Patent Document 1] PCT / US2019 / 045347 [Non-patent literature]

[0009] [Non-Patent Document 1] Gibbs-Strauss et al. Molecular imaging 10, 91-101 (2011) [Non-patent document 2] Wu et al. Journal of medicinal chemistry 51, 6682-6688 (2008) [Non-patent document 3] Wang et al. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 58, 611-621 (2010) [Non-patent document 4] Gibbs et al. PloS one 8, e73493 (2013) [Non-patent document 5] Stankoff et al. Proceedings of the National Academy of Sciences of the United States of America 103, 9304-9309 (2006) [Non-patent document 6] Cotero et al. Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging 14, 708-717 (2012) [Non-Patent Document 7] Cotero et al. PloS one 10, e0130276 (2015) [Non-patent document 8] Bajaj et al. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 61, 19-30 (2013) [Non-Patent Document 9] Gibbs-Strauss et al. Molecular imaging 9, 128-140 (2010) [Non-Patent Document 10] Meyers et al. The Journal of neuroscience : the official journal of the Society for Neuroscience 23, 4054-4065 (2003) [Non-Patent Document 11] Wang et al. The Journal of Neuroscience: the official journal of the Society for Neuroscience 31, 2382-2390 (2011) [Non-Patent Document 12] Park et al. Theranostics 4, 823-833 (2014) Summary of the Invention

[0010] One embodiment is a compound of formula (I): Provide the compound TIFF0007781065000001.tif37128, During the ceremony, R1 and R2 are each independently Straight-chain or branched C1-C6 alkyl; -(CH2) n1 -SO3 - , -(CH2) n1 -N + (CH3)3, -CH2-CH2-O-X1, -CH2-CH2-O-[CH2-CH2-O] n2 -X1, -CH2-CH2-CH2-O-X1, and -CH2-CH2-CH2-O-[CH2-CH2-CH2-O] n3 -X1; or A portion selected from the group TIFF0007781065000002.tif82131 selected from the group consisting of: R3 is hydrogen, or R2 and R3 together form a fused ring of formula (II): TIFF0007781065000003.tif36128 yields a core; R4 and R5, together with the nitrogen atom to which they are attached, forming a ring selected from the group consisting of TIFF0007781065000004.tif24128, Alternatively, when the compound is of formula (II), R4 and R5 may be independently selected from C1-C6 alkyl, with the proviso that when R1 is methyl and R4 is ethyl, R5 is not ethyl; R6 is hydrogen or Alternatively, when R2 and R3 together form a fused ring to give a core of formula (II), R5 and R6 also together with the nitrogen atom to which R5 is attached form a fused ring to give a core of formula (III): TIFF0007781065000005.tif31128 core, provided that R4 and R5, together with the nitrogen atom to which they are attached, form a ring TIFF0007781065000006.tif18128, and when R3 is H, R1 and R2 together with the nitrogen atom to which they are attached may form a pyrrolidinyl ring; X1 in each occurrence is independently selected from C1-C6 straight or branched alkyl, C1-C6 straight or branched alkenyl, C1-C6 straight or branched alkynyl, and -Si(C1-C4 alkyl)3; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and However, the sum of n2+n2 is less than or equal to 10; However, the sum of n2 + n3 is less than or equal to 10; However, the sum of n2+n4 is less than or equal to 10; However, the sum of n3 + n4 is less than or equal to 10; provided that R4 and R5 together with the nitrogen atom to which they are attached form a ring TIFF0007781065000007.tif24128, R1 and R2 are not both methyl, R1 and R2 are not both ethyl, R1 and R2 are not both n-propyl, R1 and R2 are not both n-butyl, and R1 and R2 are not both n-pentyl; and With the proviso that when the compound is of formula (III), when R1 is methyl then R4 is not methyl. [The present invention 1001] Formula (I): TIFF0007781065000008.tif37128 Compounds of: During the ceremony, R 1 and R 2 are each independently Linear or branched C 1 ~C 6 alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3-X 1 ;or TIFF0007781065000009.tif82131 A moiety selected from the group selected from the group consisting of: R 3 is hydrogen or R 2 and R 3 are taken together to form a fused ring of formula (II): TIFF0007781065000010.tif36128 Bringing the core of; R 4 and R 5 together with the nitrogen atoms to which they are attached, TIFF0007781065000011.tif24128 or forming a ring selected from the group Or, when the compound is of formula (II), R 4 and R 5 is independently C 1 ~C 6 alkyl, provided that R 4 is ethyl, R 5 is not ethyl; R 6 is hydrogen or Or, R 2 and R 3 together form a fused ring to give the core of formula (II), R 5 and R 6 Also, R 5 together with the nitrogen atom to which it is attached to form a fused ring, and the ring is represented by the formula (III): TIFF0007781065000012.tif36128 may result in a core of R 4 and R 5 together with the nitrogen atom to which they are attached form a ring TIFF0007781065000013.tif18128 and R 3 If is H, then R 1 and R 2 may be taken together with the nitrogen atom to which they are attached to form a pyrrolidinyl ring; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 More selected; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and However, the sum of n2+n2 is less than or equal to 10; However, the sum of n2 + n3 is less than or equal to 10; However, the sum of n2+n4 is less than or equal to 10; However, the sum of n3 + n4 is less than or equal to 10; However, R 4 and R 5 together with the nitrogen atom to which they are attached form a ring TIFF0007781065000014.tif24128 If R 1 and R 2 are not both methyl, and R 1 and R 2 are not both ethyl, and R 1 and R 2 are not n-propyl, and R 1 and R 2 are not both n-butyl, and R 1 and R 2 are both not n-pentyl; However, when the compound is of formula (III), R 1 If is methyl, R 4 is not methyl; and However, when the compound is of formula (III), R 1 If is ethyl, R 4 is not ethyl. [The present invention 1002] Formula (IV): TIFF0007781065000015.tif35128 and During the ceremony, R 1 and R 2 are each independently Linear or branched C 1 ~C 6 alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 ;or TIFF0007781065000016.tif82132 A moiety selected from the group selected from the group consisting of: R 3 is hydrogen or R 2 and R 3 are taken together to form a fused ring of formula (V): TIFF0007781065000017.tif36128 where n is 1 and R 3 If is H, then R 1 and R 2 may be taken together with the nitrogen atom to which they are attached to form a pyrrolidinyl ring; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 More selected; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and However, the sum of n2+n2 is less than or equal to 10; However, the sum of n2 + n3 is less than or equal to 10; However, the sum of n2+n4 is less than or equal to 10; provided that the sum of n3 + n4 is less than or equal to 10; and However, when n is 2, R 1 and R 2 are not both methyl, and R 1 and R 2 are not both ethyl, and R1 and R 2 are not n-propyl, and R 1 and R 2 are not both n-butyl, and R 1 and R 2 are not both n-pentyl, 1001 compounds of the present invention. [The present invention 1003] Formula (VI): TIFF0007781065000018.tif26128 and During the ceremony, R 1 and R 2 are each independently Linear or branched C 1 ~C 6 alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 ;or TIFF0007781065000019.tif82131 A moiety selected from the group selected from the group consisting of: R 3 is hydrogen or R 2 and R 3 are taken together to form a fused ring of formula (V): TIFF0007781065000020.tif36128 where n is 1 and R 3 If is H, then R 1 and R 2 may be taken together with the nitrogen atom to which they are attached to form a pyrrolidinyl ring; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 More selected; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and However, the sum of n2+n2 is less than or equal to 10; However, the sum of n2 + n3 is less than or equal to 10; provided that the sum of n2 + n4 is equal to or less than 10; and However, the sum of n3 + n4 is 10 or less. 1001 compounds of the present invention. [The present invention 1004] formula: TIFF0007781065000021.tif36128 and During the ceremony, R 1 teeth, Linear or branched C 1 ~C 6 alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 ;or TIFF0007781065000022.tif86131 A moiety selected from the group selected from the group consisting of: X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 More selected; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; R 4 and R 5 are each independently C 1 ~C 6 alkyl, provided that R 4 is ethyl, R 5 Isn't it ethyl? Or, R 4 and R 5 together with the nitrogen atoms to which they are attached, TIFF0007781065000023.tif24128 forming a ring selected from the group R 6 is hydrogen, provided that the sum of n2 + n4 is equal to or less than 10; and However, R 1 is methyl and R 4 is ethyl, R 5 is not ethyl, 1001 compounds of the present invention. [The present invention 1005] R 1 Is linear or branched C 1 ~C 3 1004. A compound of the present invention selected from the group of alkyl. [The present invention 1006] Formula (V): TIFF0007781065000024.tif36128 and During the ceremony, R 1 teeth, Linear or branched C 1 ~C 6 alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 ;or TIFF0007781065000025.tif82131 A moiety selected from the group selected from the group consisting of: X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 More selected; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; However, the sum of n2 + n4 is 10 or less. 1001 compounds of the present invention. [The present invention 1007] formula: TIFF0007781065000026.tif36128 The compound of the present invention 1006, having the formula: [The present invention 1008] formula: TIFF0007781065000027.tif36128 The compound of the present invention 1006, having the formula: [The present invention 1009] Formula (III): TIFF0007781065000028.tif36128 and During the ceremony, R 1 and R 2 are each independently Linear or branched C 1 ~C 6 alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O]n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 ;or TIFF0007781065000029.tif82131 A moiety selected from the group selected from the group consisting of: X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 More selected; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; However, the sum of n2+n4 is less than or equal to 10; However, R 1 is methyl, R 4 is not methyl; and However, R 1 is ethyl, R 4 is not ethyl, 1001 compounds of the present invention. [The present invention 1010] Formula (IX): TIFF0007781065000030.tif35128 wherein R 1 and R 4 are each independently C 1 ~C 6 1001. A compound of the present invention selected from alkyl. [The present invention 1011] R 1 and R 4 are each independently C 1~C 4 The compound of the present invention 1010, wherein the compound is selected from alkyl. [The present invention 1012] TIFF0007781065000031.tif32158TIFF0007781065000032.tif220158TIFF0007781065000033.tif60154 1001. A compound of the present invention selected from the group consisting of: [The present invention 1013] An imaging composition comprising an effective amount of a compound of the present invention and a pharmaceutically or physiologically acceptable carrier. [The present invention 1014] 1. A method for detecting nerves in a tissue or organ, comprising: a) administering to said tissue or organ an effective amount of a composition comprising a compound of the present invention to form a stained tissue or a stained organ; and b) imaging said stained tissue or stained organ, thereby detecting nerves intraoperatively in said stained tissue or stained organ. The method comprising: [Brief explanation of the drawings]

[0011] [Figure 1A] 1 shows the normalized absorption and fluorescence emission spectra of oxazine derivatives in PBS, for compound LGW13-79. [Figure 1B] 1 shows the normalized absorption and fluorescence emission spectra of oxazine derivatives in PBS for compound LGW14-42. [Figure 1C] 1 shows the normalized absorption and fluorescence emission spectra of oxazine derivatives in PBS for compound LGW14-47. [Figure 1D] 1 shows the normalized absorption and fluorescence emission spectra of oxazine derivatives in PBS for compound LGW14-51. [Figure 1E] 1 shows the normalized absorption and fluorescence emission spectra of oxazine derivatives in PBS for compound LGW14-53. [Figure 1F] 1 shows the normalized absorption and fluorescence emission spectra of oxazine derivatives in PBS for compound LGW14-83. [Figure 2A]Representative photographs and fluorescence images of NIR oxazine derivatives are provided following direct application of the indicated compounds (125 μM in a co-solvent formulation) to the exposed brachial plexus and sciatic nerve. [Figure 2B] Shown are the mean nerve (white), muscle (black), and adipose (gray) tissue intensities per second quantified relative to unstained controls. [Figure 2C] Quantified neural signal-to-background ratios (SBRs) calculated for comparison of the screened oxazine derivatives with the unstained control group are shown. [Figure 3A] Photographs and fluorescence images of the NIR neurospecific candidate LGW03-76 after systemic administration are provided at 0.5, 1, 2, and 4 hours. [Figure 3B] Shown are the average nerve (white), muscle (black), and adipose (gray) tissue intensities per second that were quantified and compared to control tissue autofluorescence. [Figure 3C] Quantified neural SBR calculated for comparison of LGW03-76 and control tissue autofluorescence is shown. [Figure 4A] Photographs and fluorescence images of the NIR neurospecific candidate LGW13-79 after systemic administration are provided at 0.5, 1, 2, and 4 hours. [Figure 4B] Shown are the average nerve (white), muscle (black), and adipose (gray) tissue intensities per second that were quantified and compared to control tissue autofluorescence. [Figure 4C] Quantified neural SBR calculated for comparison of LGW13-79 and control tissue autofluorescence is shown. [Figure 5A] Representative photographs and fluorescence images of the NIR neurospecific candidate LGW14-42 after systemic administration at 0.5, 1, 2, and 4 hours are provided. [Figure 5B] Shown are the average nerve (white), muscle (black), and adipose (gray) tissue intensities per second that were quantified and compared to control tissue autofluorescence. [Figure 5C] Quantified neural SBR calculated for comparison of LGW14-42 and control tissue autofluorescence is shown. DETAILED DESCRIPTION OF THE INVENTION

[0012] Detailed Description of the Invention Another embodiment is a compound of formula (IV): Provides the compound TIFF0007781065000034.tif35128, During the ceremony, R1 and R2 are each independently Straight-chain or branched C1-C6 alkyl; -(CH2) n1 -SO3 - , -(CH2) n1 -N + (CH3)3, -CH2-CH2-O-X1, -CH2-CH2-O-[CH2-CH2-O] n2 -X1, -CH2-CH2-CH2-O-X1, and -CH2-CH2-CH2-O-[CH2-CH2-CH2-O] n3 -X1; or A portion selected from the group TIFF0007781065000035.tif82131 selected from the group consisting of: R3 is hydrogen, or R2 and R3 together form a fused ring of formula (V): TIFF0007781065000036.tif36128 core, with the proviso that when n is 1 and R3 is H, R1 and R2 together with the nitrogen atom to which they are attached may form a pyrrolidinyl ring; X1 in each occurrence is independently selected from C1-C6 straight or branched alkyl, C1-C6 straight or branched alkenyl, C1-C6 straight or branched alkynyl, and -Si(C1-C4 alkyl)3; n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and However, the sum of n2+n2 is less than or equal to 10; However, the sum of n2 + n3 is less than or equal to 10; However, the sum of n2+n4 is less than or equal to 10; provided that the sum of n3 + n4 is less than or equal to 10; and With the proviso that when n is 2, R1 and R2 are not both methyl, R1 and R2 are not both ethyl, R1 and R2 are not both n-propyl, R1 and R2 are not both n-butyl, and R1 and R2 are not both n-pentyl.

[0013] Within each of the specific embodiments herein are further embodiments that provide compounds defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 are all 10 or less.

[0014] Within each of the specific embodiments herein are further embodiments that provide compounds defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 are all 8 or less.

[0015] Within each of the specific embodiments herein are further embodiments that provide compounds defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 are all 6 or less.

[0016] Within each of the specific embodiments herein, there are further embodiments that provide compounds as defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 are all 4 or less.

[0017] Within each of the specific embodiments herein, there are further embodiments that provide compounds as defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 in each group are all less than or equal to 10.

[0018] Within each of the specific embodiments herein, there are further embodiments that provide compounds as defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 in the group are all equal to or less than 8.

[0019] Within each of the specific embodiments herein, there are further embodiments that provide compounds as defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 in each group are all 6 or less.

[0020] Within each of the specific embodiments herein, there are further embodiments that provide compounds as defined by all of the variables and provisos for that specific embodiment, with the further provisos that the sum of n1+n2, the sum of n1+n3, and the sum of n1+n4 in the group are all 4 or less.

[0021] Two additional and separate embodiments relate to compounds of formula (VI) and compounds of formula (VII), respectively: Provide TIFF0007781065000037.tif29157, wherein all variables, including R1, R2, R3, X1, n, n1, n2, n3, and n4, are as defined above for formula (I), together with all provisos.

[0022] Two further separate embodiments provide compounds of formula (VI) and formula (VII), respectively, wherein in each embodiment, R3 is H, and R1 and R2 are each independently selected from the group of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, and tert-butyl.

[0023] Two further separate embodiments provide compounds of formula (VI) and formula (VII), respectively, wherein in each embodiment, R3 is H, and R1 and R2 are each independently selected from the group of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, and tert-butyl, with the proviso that R1 and R2 are not the same.

[0024] Two further separate embodiments provide compounds of formula (VI) and formula (VII), respectively, wherein in each embodiment, R3 is H, and R1 and R2 are each independently selected from the group of methyl, ethyl, n-propyl, and isopropyl, with the proviso that R1 and R2 are not the same.

[0025] Two further separate embodiments provide compounds of formula (VI) and compounds of formula (VII), respectively, wherein in each embodiment, R3 is H, R1 is selected from the group of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, and tert-butyl, and R2 is -(CH2) n1 -SO3 - , -(CH2) n1 -N + (CH3)3, -CH2-CH2-O-X1, -CH2-CH2-O-[CH2-CH2-O] n2-X1, -CH2-CH2-CH2-O-X1, and -CH2-CH2-CH2-O-[CH2-CH2-CH2-O] n3 -X1; or A portion selected from the group TIFF0007781065000038.tif82131 selected from the group consisting of: X1 in each occurrence is independently selected from C1-C6 straight or branched alkyl, C1-C6 straight or branched alkenyl, C1-C6 straight or branched alkynyl, and -Si(C1-C4 alkyl)3; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and However, when R2 is the moiety represented by k) above, the sum of n2+n4 is 10 or less.

[0026] A further embodiment is of formula (VIa): Contains compound TIFF0007781065000039.tif26128, wherein R1 and R2 are independently selected from C1 to C6 alkyl.

[0027] Another embodiment provides compounds of formula (VIa) wherein R1 and R2 are each independently selected from C1-C4 alkyl.

[0028] Another embodiment provides compounds of formula (VIa) wherein R1 and R2 are each independently selected from C1-C3 alkyl.

[0029] Another embodiment provides a compound of formula (VIa) wherein R1 is ethyl and R2 is selected from C1-C4 alkyl.

[0030] Another embodiment provides a compound of formula (VIa) wherein R1 is ethyl and R2 is selected from C1-C3 alkyl.

[0031] Another embodiment provides a compound of formula (VIa) wherein R1 is methyl and R2 is selected from C1-C4 alkyl.

[0032] Another embodiment provides a compound of formula (VIa) wherein R1 is methyl and R2 is selected from C1-C3 alkyl.

[0033] Another embodiment is of formula (II): Provides the compound TIFF0007781065000040.tif36128, wherein R1, R4, R5, R6, and all associated variables and provisos are as defined above for formula (I).

[0034] An additional embodiment provides a compound of formula (II) above, wherein R1 is as defined above for formula (I), R6 is hydrogen, and R4 and R5 are each independently selected from the group of straight-chain or branched C1-C6 alkyl, with the proviso that when R1 is methyl and R4 is ethyl, then R5 is not ethyl.

[0035] A further embodiment is of formula (VIII): Provides the compound TIFF0007781065000041.tif36128, wherein n and R1, together with all other associated variables and provisos, are as defined above for formula (I).

[0036] An additional embodiment is of formula (VIIIa): Provides the compound TIFF0007781065000042.tif36128, wherein R1, together with all other associated variables and provisos, is as defined for formula (I) above.

[0037] A further embodiment provides compounds of formula (VIIIa) above, wherein R1 is C1-C4 alkyl.

[0038] Another embodiment provides compounds of formula (VIIIa) above, wherein R1 is C1-C3 alkyl.

[0039] An additional embodiment provides compounds of formula (VIIIa) above, wherein R1 is C1-C2 alkyl.

[0040] Another further embodiment is a compound of formula (VIII b ): Provides the compound TIFF0007781065000043.tif36128, wherein R1, together with all other associated variables and provisos, is as defined for formula (I) above.

[0041] A further embodiment provides compounds of formula (VIIIb) above, wherein R1 is C1-C4 alkyl.

[0042] Another embodiment provides compounds of formula (VIIIb) above, wherein R1 is C1-C3 alkyl.

[0043] An additional embodiment provides compounds of formula (VIIIb) above, wherein R1 is C1-C2 alkyl.

[0044] Yet a further embodiment is a compound of formula (III): Provides the compound TIFF0007781065000044.tif36128, wherein R1 and R4, together with all other associated variables and provisos, are as defined for formula (I) above, with the proviso that when R1 is methyl, R4 is not methyl, and with the proviso that when R1 is ethyl, R4 is not ethyl.

[0045] Another embodiment provides a compound of formula (III) above, wherein R1 is C1-C6 alkyl and R4 is as defined for formula (I) above, together with all other associated variables and provisos, with the proviso that when R1 is methyl, R4 is not methyl, and when R1 is ethyl, R4 is not ethyl.

[0046] Another embodiment provides a compound of formula (III) above, wherein R1 is C1-C4 alkyl and R4 is as defined for formula (I) above, together with all other associated variables and provisos, with the proviso that when R1 is methyl, R4 is not methyl, and with the proviso that when R1 is ethyl, R4 is not ethyl.

[0047] Another embodiment provides a compound of formula (III) above, wherein R1 is C1-C3 alkyl and R4 is as defined for formula (I) above, together with all other associated variables and provisos, with the proviso that when R1 is methyl, R4 is not methyl, and with the proviso that when R1 is ethyl, R4 is not ethyl.

[0048] Another embodiment provides a compound of formula (III) above, wherein R1 is C1-C2 alkyl and R4 is as defined for formula (I) above, together with all other associated variables and provisos, with the proviso that when R1 is methyl, R4 is not methyl, and when R1 is ethyl, R4 is not ethyl.

[0049] Yet another embodiment provides a compound of formula (III) above, wherein R1 and R2 are each independently selected from C1-C6 alkyl, with the proviso that when R1 is methyl, R4 is not methyl, and with the proviso that when R1 is ethyl, R4 is not ethyl.

[0050] A further embodiment provides a compound of formula (III) above, wherein R1 and R2 are each independently selected from C1-C4 alkyl, with the proviso that when R1 is methyl, R4 is not methyl, and with the proviso that when R1 is ethyl, R4 is not ethyl.

[0051] Another embodiment provides a compound of formula (III) above, wherein R1 and R2 are each independently selected from C1-C3 alkyl, with the proviso that when R1 is methyl, R4 is not methyl, and with the proviso that when R1 is ethyl, R4 is not ethyl.

[0052] An additional embodiment is of formula (IX): TIFF0007781065000045.tif35128, wherein R1 and R4 are each independently selected from C1-C6 alkyl.

[0053] A further embodiment provides compounds of formula (IX) wherein R1 and R4 are each independently selected from C1-C4 alkyl.

[0054] Another embodiment provides a compound of formula (IX) wherein R1 and R4 are each independently selected from C1-C3 alkyl.

[0055] A further embodiment provides compounds of formula (IX) wherein R1 and R4 are each independently selected from C1-C2 alkyl.

[0056] A further embodiment provides compounds of formula (IX), wherein R 1 is as defined for formula (I) above, along with all defined associated variables and provisos.

[0057] definition "Subject" or "patient" refers to any animal. The animal may be a mammal. Examples of suitable mammals include humans and non-human primates, dogs, cats, sheep, cows, pigs, horses, mice, rats, rabbits, and guinea pigs. In some embodiments, the subject or patient is a human, particularly including a human undergoing or in need of a surgical procedure or examination.

[0058] As used herein, the term "nerve" refers to a bundle of nerve axons. Within a nerve, each axon is surrounded by a layer of connective tissue called the endoneurium. The axons are organized into groups called fascicles, and each fascicle is surrounded by a layer of connective tissue called the perineurium. The entire nerve is surrounded by a layer of connective tissue called the epineurium. The term "nerve" refers to any tissue (e.g., the sinus node or chamber The term "neuromuscular junction" is intended to include the muscular junction (neuronal nodes) or their associated structures (e.g., neuromuscular junctions).

[0059] As used herein, the terms "nerve-specific" or "nerve specific" refer to an agent that is attracted to nerves or nerve tissue and can be used in fluorescent imaging techniques to help contrast and distinguish nerves or nerve tissue from surrounding cells and / or tissues. The term "neuronal specificity" refers to the property or activity of an agent that is neurospecific.

[0060] The term "near-infrared" or the acronym "(NIR)" generally refers to light in the near-infrared spectrum, which generally has wavelengths from about 0.65 to about 1.4 μm (700 nm to 1400 nm). It may also refer to the range designated by the International Organization for Standardization, which has wavelengths from about 0.78 μm to about 3 μm. In some embodiments, the preferred near-infrared spectroscopy and imaging (NIRS) range is from about 650 nm to about 950 nm. In other embodiments, the preferred near-infrared spectroscopy and imaging (NIRS) range is from about 650 nm to about 900 nm.

[0061] In some embodiments, the active substance and / or the composition comprising it are intended for direct / local administration.Direct or local administration is understood herein to include the direct administration of the active substance or composition to the surface of tissue, organ, nerve bundle or other body component.In some methods, administration can be achieved by brushing, spraying or irrigating with the appropriate compound or composition.

[0062] In another embodiment, the agents and / or compositions may be administered systemically to the patient or subject, such as through intravenous injection or infusion.

[0063] In another embodiment, the agents and / or compositions may be administered locally to the desired tissue or organ, such as via injection.

[0064] The term "effective amount" or "medically effective amount" or "imaging effective amount" or similar terms refers to an amount of a compound or composition described herein that sufficiently covers the target area to complete binding to one or more nerves such that the compound or composition described herein can be identified through relevant imaging techniques, particularly near-infrared imaging techniques.

[0065] The term "alkyl" refers to a straight-chain or branched hydrocarbon. For example, an alkyl group may contain 1 to 6 carbon atoms (i.e., C1-C6 alkyl or C 1~6 alkyl), 1 to 4 carbon atoms (i.e., C1 to C4 alkyl or C 1~4 alkyl), 1 to 3 carbon atoms (i.e., C1 to C3 alkyl or C 1~3 alkyl), or 1-2 carbon atoms (i.e., C1-C2 alkyl or C 1~2Examples of suitable alkyl groups include methyl, ethyl, n-propyl, isopropyl (-CH(CH3)2), 1-butyl (n-Bu, n-butyl, --CH2CH2CH2CH3), 2-methyl-1-propyl (i-Bu, i-butyl, --CH2CH(CH3)2), 2-butyl (s-Bu, s-butyl, --CH(CH3)CH2CH3), 2-methyl-2-propyl (t-Bu, t-butyl, --C( CH3)3), 1-pentyl (n-pentyl, --CH2CH2CH2CH2CH3), 2-pentyl (--CH(CH3)CH2CH2CH3), 3-pentyl (--CH(CH2CH3)2), 2-methyl-2-butyl (-C(CH3)2CH2CH3), 3-methyl-2-butyl (--CH(CH3)CH(CH3)2), 3-methyl-1-butyl (--CH2CH2CH(CH3)2), 2-Methyl-1-butyl (-CH2CH(CH3)CH2CH3), 1-hexyl (--CH2CH2CH2CH2CH2CH2CH3), 2-hexyl (--CH(CH3)CH2CH2CH2CH2CH3), 3-hexyl (-CH(CH2CH3)(CH2CH2CH3)), 2-methyl-2-pentyl (-C(CH3)2CH2CH2CH3), 3-methyl-2-pentyl (-CH(CH3)CH(C H3)CH2CH3), 4-methyl-2-pentyl (-CH(CH3)CH2CH(CH3)2), 3-methyl-3-pentyl (--C(CH3)(CH2CH3)2), 2-methyl-3-pentyl (-CH(CH2CH3)CH(CH3)2), 2,3-dimethyl-2-butyl (--C(CH3)2CH(CH3)2), and 3,3-dimethyl-2-butyl (-CH(CH3)C(CH3)3 ) This includes, but is not limited to:

[0066] The term "alkenyl" refers to an alkyl group having at least one site of unsaturation, i.e., a carbon-carbon sp 2 It refers to a straight or branched chain hydrocarbon having a double bond. For example, an alkenyl group can have 2 to 4 carbon atoms (i.e., C2-C4 alkenyl). )Examples of suitable C2-C4 alkenyl groups include, but are not limited to, ethenyl or vinyl (-CH=CH2), allyl (-CH2CH=CH2), but-1-enyl (-CH=CH-CH2-CH3), but-2-enyl (CH2-CH=CH-CH3), but-3-enyl (-CH2-CH2-CH=CH).

[0067] The term "alkynyl" refers to a straight-chain or branched hydrocarbon having at least one site of unsaturation, i.e., a carbon-carbon sp triple bond. For example, an alkynyl group can have 2 to 6 carbon atoms (i.e., a C2-C6 alkyne) or 2 to 4 carbon atoms (i.e., a C2-C4 alkynyl). Examples of suitable alkynyl groups include, but are not limited to, acetylene (-C≡CH), propargyl (-CH2C≡CH), and the like.

[0068] It is also understood that the compound structures generally and specifically described and / or depicted herein include all corresponding resonance structures for such compounds. As an example using the structures below, compound A may be referred to as 3-(dimethyl-14-azaneilidene)-7-(pyrrolidin-1-yl)-3H-phenoxazine, and compound B may be referred to as N,N-dimethyl-7-(114-pyrrolidin-1-ylidene)-3H-715-phenoxazin-3-amine, each falling within the present definition of a compound of formula (I) in which R1 and R2 form a pyrrolidinyl ring, R4 and R5 are each methyl, and R3 and R6 are both hydrogen, and each of compound structures A, B, C, and D includes and represents the others herein. TIFF0007781065000046.tif83130

[0069] The term "imaging" as used herein refers to the use of fluorescent compounds in conventional medical imaging techniques, including, but not limited to, those associated with fluorescence image-guided surgery (including minimally invasive laparoscopy or endoscopic techniques), computer-assisted surgery or surgical navigation, radiosurgery or radiotherapy, interventional imaging, fluorescence microscopy, and laser confocal microscopy, which may involve near-infrared wavelengths between about 650 nm and 900 nm.

[0070] The term "label" refers to a molecule that facilitates visualization and / or detection of a target molecule disclosed herein. In some embodiments, the label is a fluorescent moiety. The term "labeling" refers to the successful administration of a label to a target to enable such detection.

[0071] As used herein, the terms "robotic surgery," "robotic-assisted surgery," or "computer-assisted surgery" refer to surgical techniques involving robotic systems that control the movement of medical instruments to perform surgical procedures with precise, flexible, and / or minimally invasive actions designed to limit the amount of surgical trauma, blood loss, pain, scarring, and post-operative patient recovery time, and / or complications such as infection at the surgical site. Examples of robotic surgery include those performed using the da Vinci Surgical System (Intuitive Surgical, Sunnyvale, CA, USA), which was approved by the U.S. Food and Drug Administration in 2000.

[0072] As used herein, the term "surgery" or "surgical procedure" refers to any method used to manipulate, alter, or produce an effect by physical intervention. These methods include, but are not limited to, open surgery, endoscopic surgery, laparoscopic surgery, minimally invasive surgery, robotic surgery, and any procedure that may affect neurons or nerves, such as placement of a retractor during spinal surgery, conductive cardiac tissue or nerve ablation, epidural injections, intrathecal injections, neuronal or nerve blocks, implantation of devices such as neuronal or neurostimulators, and pump implantation. These methods may also include biopsies or other invasive techniques for collection of cell or tissue samples, such as for diagnostic purposes.

[0073] As used herein, the term "target molecule" refers to any agent (e.g., peptide, protein, nucleic acid polymer, aptamer, or small molecule) that associates with (e.g., binds to) a target of interest. The target of interest may be a nerve cell, or an organ or tissue associated with one or more nerve cells or nerve structures. In some embodiments, the target molecule is any agent that associates with (e.g., binds to) a target comprising one or more neurons, nerves, or tissues or structures associated therewith, i.e., nerve tissue, nervous system tissue, nerve bundles, etc. Nerve and nerve-related targets are understood to include those associated with the brain and spinal cord of the central nervous system (CNS) and nerves of the peripheral nervous system (PNS).

[0074] The term "prostatectomy" refers to a surgical technique for removing all or part of a subject's prostate gland. A "radical prostatectomy" involves the removal of a subject's entire prostate gland along with surrounding tissue, often including the seminal vesicles and nearby lymph nodes.

[0075] The terms "orthopedic limb repair" or "orthopedic limb repair surgery" refer to surgical techniques performed on the musculoskeletal system of a subject's limb. These techniques include limb reconstruction surgery, joint replacement procedures, joint revision surgery, debridement, bone fusion, tendon or ligament repair, bone internal fixation, and osteotomy.

[0076] The term "fluorophore" as used herein refers to any one of the compounds described herein for use in imaging techniques, particularly neuroimaging techniques. Each of the compounds described herein as the product of a specific synthesis or described in the general description is considered a fluorophore for the methods, uses, and compositions.

[0077] The term "variable" or "variables" as used herein in the general description and claims refers to an entity or moiety that may be selected from a particular group, as the case may be. Such variables may include R, R, R, R, R, R, R, n, n, n, n, X, etc.

[0078] All ranges disclosed and / or claimed herein are inclusive of the recited endpoints and are independently combinable (e.g., the ranges "from 2 to 10" and "2-10" include the endpoints 2 and 10 and all intermediate values). For example, reference to "claims 2-5" includes claims 2, 3, 4, and 5.

[0079] The term "intra-operative" as used in describing methods or uses herein refers to activities that take place during a surgical procedure or in close temporal preparation for such a procedure.

[0080] As used herein, terms such as "pharmaceutically acceptable" or "physiologically acceptable" when used with respect to a formulation or composition component refer to a pharmaceutically acceptable vehicle, including, but not limited to, any and all carriers, solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like. Such materials provide an acceptable level of activity for the fluorophore / compound in question, and are compatible with and substantially non-toxic to cells, tissues, organs, and the like with which they come into contact. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions.

[0081] The term "carrier" refers to an excipient or vehicle, including, but not limited to, diluents, disintegrants, anti-precipitation agents, surfactants, glidants, emulsifiers, buffers, stabilizers, lubricants, etc., with which the compound of interest is administered. Carriers are also reviewed herein and in "Remington's Pharmaceutical Sciences" by E.W. Martin. However, it should be understood that the carrier selected for a pharmaceutical composition, and the amount of such carrier in the composition, may vary depending on the formulation method.

[0082] The term "diluent" generally refers to a substance used to dilute a compound of interest prior to delivery.

[0083] How to use 1. A method for detecting nerves in a tissue or organ, comprising: a) administering to a tissue or organ an effective amount of a composition comprising a fluorophore as described herein to form a stained tissue or a stained organ; and b) imaging the stained tissue or stained organ, thereby detecting nerves intraoperatively in the stained tissue or stained organ; A method is provided, comprising:

[0084] 1. A method for intraoperative nerve detection in a subject undergoing surgery, comprising: c) administering to a subject an effective amount of a composition comprising a fluorophore described herein before or during surgery to form stained tissue; and d) imaging the stained tissue in the subject undergoing surgery, thereby detecting nerves intraoperatively in the subject undergoing surgery. A method is provided, comprising:

[0085] 1. A method for intraoperative nerve detection in a subject undergoing prostatectomy surgery, comprising: e) administering to a subject an effective amount of a composition comprising a fluorophore described herein before or during prostatectomy surgery to form stained tissue; and f) imaging stained tissue undergoing surgery in the subject, thereby detecting nerves intraoperatively in the subject undergoing prostatectomy surgery. A method is also provided, including:

[0086] In one embodiment, a method for detecting cavernous nerves intraoperatively in a subject undergoing prostatectomy surgery, comprising: g) administering to a subject an effective amount of a composition comprising a fluorophore described herein before or during prostatectomy surgery to form stained tissue; and h) imaging the stained tissue undergoing surgery in the subject, thereby detecting cavernous nerves intraoperatively in the subject undergoing prostatectomy surgery. A method is provided, comprising:

[0087] For each of the methods herein that relate to a prostatectomy surgery or procedure, there is another embodiment in which the surgery or procedure is a radical prostatectomy.

[0088] For each of the methods described above and herein, there are embodiments in which the composition comprising the fluorophore is administered systemically to the subject.

[0089] For each of the methods described above and herein, there are embodiments in which the composition comprising the fluorophore is administered directly or topically, i.e., via direct or topical administration, to the subject.

[0090] Within each of the methods herein, there are further embodiments in which administering an effective amount of a composition comprising a fluorophore as described herein to a subject before or during a prostatectomy procedure to form stained tissue can be completed in 15 minutes or less. In still further embodiments, administering an effective amount of a composition comprising a fluorophore as described herein to a subject before or during a prostatectomy procedure to form stained tissue can be completed in 10 minutes or less.

[0091] Also provided herein are methods of imaging neural tissue tumors (neoplasms), including gliomas such as gliomatosis cerebri, oligoastrocytoma, choroid plexus papilloma, ependymoma, astrocytoma (pilocytic astrocytoma and glioblastoma multiforme), dysembryonic neuroepithelial tumor, oligodendroglioma, medulloblastoma, and primitive neuroectodermal tumor; neuroepithelioma tumors such as ganglioneuroma, neuroblastoma, atypical teratoma, retinoblastoma, and nasal neuroblastoma; and nerve sheath tumors such as neurofibroma (neurofibrosarcoma and neurofibromatosis), schwannoma, schwannoma, acoustic neuroma, and neuroma.

[0092] Provided is a method for imaging a target area in a subject, the method comprising contacting the target area in the subject with a compound selected from the compounds herein, and detecting the compound in the target using fluorescence or near-infrared imaging.

[0093] Also provided is a method for imaging one or more nerves in a target region in a subject, the method comprising contacting the target region in the subject with a compound selected from the compounds herein, and detecting the compound in the target using fluorescent imaging.

[0094] Also provided is a method for imaging one or more nerves in a target region in a subject, the method comprising contacting the target region in the subject with a compound selected from the compounds herein, and detecting the compound in the target using near-infrared imaging.

[0095] 1. A method of minimizing nerve damage in a target area in a subject during a medical procedure, comprising: a) contacting a target area in a subject with a compound selected from the compounds described herein; b) detecting one or more nerves bound by the compound in the target area using fluorescent imaging; and c) minimizing the effects of medical procedures that may damage the detected nerve or nerves A method is also provided, including:

[0096] The above methods may be used to identify nerves and minimize damage to nerves, including traumatic, thermal, and radiation damage that may be caused by medical procedures, or damage to nerves caused by the application of therapeutic agents, anesthetics, or anesthesia in a target area.

[0097] In some embodiments, the medical procedure referred to in the above method is a surgical procedure. In another embodiment, the medical procedure is a biopsy procedure, a radiation treatment, or the administration of an anesthetic or anesthesia to a subject. In a further embodiment, the medical procedure in the above method is the insertion or implantation of a medical device, including a medical pump, a stent, a pacemaker, a port, an artificial joint, a valve, a screw, a pin, a plate, a rod, a cosmetic implant, a neurostimulator, etc.

[0098] Also provided is the use of any compound disclosed herein in the preparation of a composition for use in imaging one or more nerves in a subject using near-infrared imaging.

[0099] Nerve injury impairs surgical outcomes and significantly impacts postoperative quality of life. Despite decades of nerve-sparing techniques, identifying and preserving nerves during surgery remains challenging, with success rates strongly correlated with the surgeon's experience and ability to master the technique (Walsh & Donker, The Journal of Urology 128, 492-497 (1982); Ficarra et al., Eur Urol 62, 405-417 (2012); Damber & Khatami, Acta Oncologica 44, 599-604 (2005)). Fluorescence-guided surgery (FGS) holds promise for improving visualization by specifically highlighting tissues, such as nerves and tumor tissue, during surgery. Using optical imaging techniques, FGS enables sensitive and specific real-time wide-field identification of target tissues from tissue-targeted fluorescent probes. For example, Frangioni. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 26, 4012-4021 (2008); Gibbs. Quantitative imaging in medicine and surgery 2, 177-187 (2012); Gioux et al. Molecular imaging 9, 237-255 (2010); Vahrmeijer et al. Nature reviews. Clinical oncology 10, 507-518 (2013); and Nguyen et al. Nature reviews. Cancer 13, 653-662 (2013) 1~5See, FGS technology, which operates in the near-infrared (NIR) optical window (wavelengths of 650-900 nm), where tissue chromophore absorbance, autofluorescence, and scattering are minimal, has the ability to identify target tissue at depths of millimeters to centimeters against a black background (Chance. Annals of the New York Academy of Sciences 838, 29-45 (1998); Gibbs. Quantitative imaging in medicine and surgery 2, 177-187 (2012)).

[0100] Several imaging systems have been developed for FGS applications. For example, Lee et al. Plastic and reconstructive surgery 126, 1472-1481 (2010); Tummers et al. European journal of surgical oncology: the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology 40, 850-858 (2014); Troyan et al. Annals of surgical oncology 16, 2943-2952 (2009); Ashitate et al. Real-time simultaneous near-infrared fluorescence imaging of bile duct and arterial anatomy. The Journal of surgical research 176, 7-13 (2012); Verbeek et al. The Journal of urology 190, 574-579 (2013); Gibbs-Strauss et al. Molecular imaging 10, 91-101 (2011); Hirche et al. Surgical innovation 20, 516-523 (2013); Gotoh et al. Journal of surgical oncology 100, 75-79 (2009); and Kitagawa et al. Anticancer research 35, 6201-6205 (2015). 。 Importantly, the da Vinci surgical robot, which is frequently used for robotic-assisted radical prostatectomy (RP), can be fitted with an FDA-approved fluorescence imaging channel.

[0101] Direct administration (also known as local administration) is an attractive alternative to systemic administration of fluorescent probes because it minimizes potential toxicity and reduces the initial regulatory burden in human clinical studies. By selectively labeling tissue within the surgical field, direct administration requires a much lower dose than systemic administration. A direct administration method was developed that yields a nerve signal-to-background ratio (SBR) equivalent to that of systemic administration after a 15-minute staining protocol. Barth & Gibbs. Theranostics 7, 573-593 (2017). This methodology was successfully applied to an autonomic nervous system model that successfully mimics the nerves surrounding the prostate. This method has additional advantages in RP applications, as nerve labeling via systemic administration during RP can result in unacceptably high background from nerves in the prostate and renal fluorophore clearance, which would generate a significant fluorescent signal in the urine of the adjacent bladder. Both of these extraneous fluorescent signals would reduce the ability to identify cavernous nerves within the neurovascular bundle (NVB), which is involved in urination and sexual performance (Barth and Summer. Theranostics (2016). Tewari et al. BJU International 98, 314-323 (2006); Patel et al. Eur Urol 61, 571-576 (2012)). Perhaps most importantly, direct administration requires a dose 16-fold lower than systemic administration, and when scaled to humans by body surface area, the dose falls within the range required for clinical application under an Exploratory Investigational New Drug (eIND) application to the FDA. In studies conducted under eIND, each patient receives only a microdose (<100 μg), requiring minimal preclinical toxicology testing and significantly reducing the cost of first-in-human trials.

[0102] Direct administration has resulted in high neurospecificity and SBR with short staining protocols in preclinical rodent models (Barth & Gibbs, Theranostics 7, 573-593 (2017)), but preliminary staining studies in large animal models have yielded significant background. To facilitate clinical application, improved formulation strategies will be required that are FDA-approved and facilitate increased application control for staining various tissue surfaces, angles, and morphologies.

[0103] Formulations containing one or more of the compounds disclosed herein can be used to image nerves or nerve tissue. In certain embodiments, the disclosed formulations can be used to image nerves or nerve tissue in a subject. In certain embodiments, images of the nerves can be acquired intraoperatively during FGS. In certain embodiments, visualization of the nerves during FGS allows surgery to be performed on the target tissue while sparing the nerves, reducing the incidence of nerve damage during surgery. The area where the surgery will be performed or nearby areas can be exposed during surgery. The surgery can be performed on organs, including tissues such as nerve tissue, muscle tissue, and fat tissue. The surgery can be performed laparoscopically, which is minimally invasive and involves the use of a thin, tubular instrument (laparoscope) inserted through a keyhole-shaped incision into a part of the subject's body, such as the abdomen or pelvis. The surgery can be robotically assisted. Robotically assisted surgery can provide greater precision, flexibility, and control and is often associated with minimally invasive surgery.

[0104] In certain embodiments, the fluorophore concentration in formulations to be applied directly to neural tissue includes a concentration range of 40-300 μg / mL. In certain embodiments, the fluorophore concentration in formulations for direct application includes 40 μg / mL, 50 μg / mL, 60 μg / mL, 70 μg / mL, 80 μg / mL, 90 μg / mL, 100 μg / mL, 110 μg / mL, 120 μg / mL, 130 μg / mL, 140 μg / mL, 150 μg / mL, 160 μg / mL, 170 μg / mL, 180 μg / mL, 190 μg / mL, and 200 μg / mL. In certain embodiments, the fluorophore concentration in formulations for direct application is 50 μg / mL. In certain embodiments, the fluorophore concentration in formulations for direct application is 200 μg / mL.

[0105] The disclosed formulations can be applied systemically to a subject for neuroimaging, hi certain embodiments, systemic application of the formulation comprises intravenous injection of the formulation into a subject.

[0106] Formulations applied directly to tissues can be allowed to penetrate the tissue for a given period of time after direct application. In certain embodiments, the formulation can be allowed to penetrate the tissue for 30 seconds to 15 minutes, 1 to 10 minutes, 1 to 5 minutes, 1 minute, 2 minutes, 3 minutes, 4 minutes, or 5 minutes. In certain embodiments, the formulation can be allowed to penetrate the tissue for 1 to 2 minutes. Formulations applied systemically to a subject can be administered long enough before imaging to allow the formulation to reach the area to be imaged and be present in such area upon imaging. In certain embodiments, formulations applied systemically to a subject can be administered long enough prior to imaging to allow uptake of the formulation by the tissues in the subject. In certain embodiments, the formulation can be administered up to 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 7 hours, or 8 hours before imaging, or less than 30 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 7 hours, or 8 hours before imaging. The required time may vary depending on the neuroimaging application and the administration site. In certain embodiments, the formulation is administered within 30 minutes, 1 hour, 2 hours, 3 hours, or 4 hours prior to imaging. In certain embodiments, the formulation is administered within 2 hours prior to imaging.

[0107] Tissues stained with a formulation containing a fluorophore via direct application can be washed with a buffer solution prior to imaging the stained tissue. Washing tissues stained with a formulation containing a fluorophore can include rinsing the tissue with an appropriate buffer solution to remove the buffer solution. In certain embodiments, the stained tissue can be washed 1-18 times, 1-10 times, 1-6 times, 1 time, 2 times, 3 times, 4 times, 5 times, or 6 times with the wash buffer. In certain embodiments, the stained tissue can be washed 6 times. In certain embodiments, the wash buffer is phosphate-buffered saline (PBS). In certain embodiments, washing the stained tissue removes unbound fluorophore. In certain embodiments, washing the stained tissue increases neural signal intensity and / or signal-to-background ratio (SBR) compared to not washing the stained tissue. In certain embodiments, washing the stained tissue redissolves the fluorophore, allowing for further diffusion of the fluorophore into the neural tissue.

[0108] Imaging tissue stained with a formulation containing a fluorophore involves irradiating the tissue stained with the disclosed formulation with light. The light can be of a wavelength sufficient to excite the fluorophore in the formulation and cause it to fluoresce. In certain embodiments, the light for exciting the fluorophore is at a wavelength in the near-infrared spectrum. In certain embodiments, the fluorophore in the formulation emits light at a wavelength in the near-infrared spectrum. In certain embodiments, the near-infrared spectrum includes wavelengths from 650 nm to 900 nm. In some embodiments, the infrared spectrum of interest is about 700 nm. In other embodiments, the infrared spectrum of interest includes wavelengths from about 725 nm to about 875 nm.

[0109] Imaging tissue stained with a formulation comprising a fluorophore includes obtaining a fluorescent image of the stained tissue with an optical imaging system such as those described in the Examples.

[0110] In certain embodiments, imaging the tissue involves observing a fluorescent image of the stained tissue. The fluorescent image may include a still image (printed or on a screen) or a real-time image on a video monitor. In certain embodiments, individual images of nerves obtained by staining the nerves with the formulations can be used for diagnostic purposes and to describe the nerve's location. By observing the fluorescent image, the surgical team can determine the presence or absence of nerves in the image. Thus, the surgical team can use information regarding the presence or location of one or more nerves to determine how to perform a surgical procedure. For example, based on information obtained through the disclosed methods, the surgical team may determine to perform a surgical cut at a point in the tissue where a particular nerve is less likely to be inadvertently severed or contacted during surgery, based on the knowledge that no nerves are present in the region of the tissue.

[0111] Information gained from the resulting images can be useful for reconnecting nerve endings if they have been severed. In the case of a transection, a nerve splice can be applied directly to the end to stimulate the sprouting of regenerating nerve fibers. In this case, the light visible from the fluorescence of the severed nerve end provides a target for guiding the nerve anastomosis with the nerve splice.

[0112] Formulations are provided that include an effective amount of a compound described herein and a pharmaceutically or physiologically acceptable carrier. In some embodiments, the pharmaceutically or physiologically acceptable carrier is an aqueous carrier.

[0113] Aqueous carriers may include saline solutions, such as buffered saline solutions, and aqueous dextrose and glycerol solutions. Suitable pharmaceutical carriers may also contain excipients such as glucose, lactose, sucrose, glycerol monostearate, sodium chloride, glycerol, propylene, glycol, water, ethanol, and the like. The composition, if desired, can also contain minor amounts of wetting or emulsifying agents (such as the KOLLIPHOR® line of products available from BASF) or pH buffering agents.

[0114] The disclosed formulations for detecting neural tissue can also be provided as kits. A kit for detecting neural tissue can include (i) an aqueous formulation containing a fluorophore and (ii) one or more wash buffers in separate containers. The kit can include a notice in a format prescribed by a government agency regulating the manufacture, use, or sale of pharmaceuticals or biological products, reflecting approval by the agency for manufacture, use, or sale for human administration. The notice can state that the provided active ingredient can be administered to a subject. The kit can include additional instructions for using the kit, such as instructions for applying the formulation directly to the tissue; removing excess formulation by washing; administering the formulation systemically to the subject; irradiating the tissue with light to visualize the fluorophore; capturing a fluorescent image of the tissue; and properly disposing of associated waste. The instructions can be in the form of printed instructions provided within the kit, or the instructions can be printed on a part of the kit itself. The instructions can be in the form of a sheet, pamphlet, booklet, CD-ROM, or computer-readable device, or can provide directions to instructions at a remote location, such as a website. In certain embodiments, the kits may also include some or all of the necessary laboratory and / or medical supplies required to effectively use the kit, such as syringes, ampoules, tubes, gloves, tubing, buffers, etc. The contents of any kit described herein may be varied.

[0115] Overview All reagents were purchased from Sigma-Aldrich, Fisher Scientific, or TCI. Unless otherwise indicated, all commercially available starting materials were used as is without further purification. Analytical TLC was performed on Millipore ready-to-use plates with silica gel 60 (F254, 32–63 μm). Purification was performed on a Biotage Isolera Flash System using prepacked silica gel cartridges or on a reverse-phase preparative HPLC (Agilent 1250 Infinity HPLC).

[0116] LCMS characterization The mass-to-charge ratio and purity of the oxazine compounds were characterized on an Agilent 6244 time-of-flight LCMS equipped with a diode array detector VL+. Samples (10 μL) were injected onto a C18 column (Poroshell 120, 4.6 × 50 mm, 2.7 μm) and analyzed by elution with A (HO, 0.1% FA) and B (MeCN, 0.1 The elution was performed at 0.4 mL / min with a solvent system of 90 / 10% FA (A / B = 90 / 10 to 5 / 95 for 10 min, maintained at A / B = 5 / 95 for an additional 5 min. Ions were detected in positive ion mode by setting the capillary voltage at 4 kV and the gas temperature at 350 °C.

[0117] Neurospecific screening using direct / local administration Compounds were screened for tissue specificity in the mouse brachial plexus and sciatic nerve using previously published direct / local administration strategies. 6 Each compound from the oxazine library was formulated at 125 μM in a previously utilized cosolvent formulation (10% DMSO, 5% Kolliphor, 65% serum, and 20% phosphate-buffered saline). 100 μL of the oxazine formulation was incubated on the exposed brachial plexus or sciatic nerve for 5 minutes. The fluorophore-containing solution was removed, and the area was irrigated 18 times with saline to remove all unbound fluorophore. Registered fluorescence and color images of each stained area were collected 30 minutes after direct / topical administration of oxazine using a custom-built macroscopic imaging system equipped with 620 / 60 nm excitation and 700 / 75 nm emission bandpass filters. Using custom-built MatLab code, tissue-specific fluorescence was analyzed by selecting regions of interest for nerve, muscle, and adipose tissue using white-light images. These regions of interest were then analyzed on the registered and matched fluorescence images to assess nerve-to-muscle and nerve-to-fat ratios.

[0118] Neurospecific screening using systemic administration Compounds were screened for tissue specificity in the mouse brachial plexus and sciatic nerve using previously published systemic administration strategies. 6 Each compound from the oxazine library was formulated at 2 mM in a previously utilized cosolvent formulation (10% DMSO, 5% Kolliphor, 65% serum, and 20% phosphate-buffered saline). 100 μL of the oxazine formulation was administered intravenously 4 h before exposure of the brachial plexus and sciatic nerve. Registered fluorescence and color images of each nerve site were collected using a custom-built macroscopic imaging system equipped with 620 / 60 nm excitation and 700 / 75 nm emission bandpass filters. Using custom-built MatLab code, tissue-specific fluorescence was analyzed by selecting regions of interest for nerve, muscle, and adipose tissue using white-light images. These regions of interest were then analyzed on the registered and matched fluorescence images to blindly assess nerve-to-muscle and nerve-to-fat ratios.

[0119] chemical synthesis TIFF0007781065000047.tif96128 Scheme Synthetic route to LGW11-98. Reagents and conditions: a) 6M HCl, NaNO2, 0°C; b) chloroacetic acid chloride, TBAB, NaHCO3, HO, 0°C; c) 1M BBr3, DCM, 0°C to room temperature; d) NaH, THF, 0°C to room temperature; e) BH3-THF, THF, 0°C to room temperature; f) Ac2O, HO, 50°C to room temperature; g) BH3-THF, THF, 0°C to room temperature; h) Compound 2, HClO4, 90% i-PrOH, 80°C.

[0120] 5-(Dimethylamino)-2-nitrosophenol (2): Compound 1 (1.00 g, 7.29 mmol) was dissolved in ice-cold 6 M HCl solution (5 mL). To the above solution, NaNO (0.513 g, 7.44 mmol) was added portionwise over 1 h, maintaining the solution temperature below 5 °C so that brown NO vapors were not observed. The reaction mixture was stirred for an additional 2 h. After this time, the precipitate was filtered through a Buchner funnel and washed with small portions of ice-cold 2 M HCl solution. The product was left in the funnel and air-dried overnight to give compound 2 (1.01 g, 84%) as a yellow solid, which was used in the next step without further purification.

[0121] 2-Chloro-N-(2,5-dimethoxyphenyl)acetamide (4): Compound 3 (20.0 g, 130 mmol) was dissolved in anhydrous MeCN (60 mL) under N and cooled in an ice bath. To this solution, EtN (40 mL, 287 mmol) and chloroacetic acid chloride (12.7 mL, 159 mmol) were carefully added. The reaction mixture was stirred for 1 h and then diluted with 500 mL of DI water. The solid suspension was filtered to give compound 4 (21.0 g, 70%) as a light brown solid, which was used in the next step without further purification.

[0122] 2-Chloro-N-(2,5-dihydroxyphenyl)acetamide (5): Compound 4 (10.0 g, 43.5 mmol) was dissolved in anhydrous DCM (20 mL) under N2 and cooled in an ice bath. To the above solution, BBr3 (1 M in DCM, 130 mL, 130 mmol) was added dropwise over 1 h using a syringe pump. The reaction mixture was allowed to warm slowly to room temperature and stirred overnight. The reaction flask was placed in an ice bath, and after sufficient cooling time, water was carefully added to the reaction mixture to quench excess BBr3. The resulting precipitate was collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 5 (7.96 g, 91%), which was used in the next step without further purification.

[0123] 6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one (6): Compound 5 (6.00 g, 29.8 mmol) was dissolved in anhydrous THF (50 mL) under N and cooled in an ice bath. After sufficient cooling time, NaH (60%, 4.17 g, 104 mmol) was added to the solution in four portions over 10 minutes. The reaction mixture was allowed to warm slowly to room temperature and stirred overnight. Upon completion of the reaction, ice-cold water was carefully added to the reaction flask to quench the excess NaH. The reaction mixture was acidified with 2 M HCl and subsequently extracted with EtOAc (5 × 100 mL). The combined organic layers were rinsed with brine and dried over anhydrous NaSO. The solvent was removed using a rotary evaporator, and the residue was purified by flash column chromatography on silica gel using EtOAc / DCM / hexane as eluent to give compound 6 (3.12 g, 63%) as a light brown solid.

[0124] 3,4-Dihydro-2H-benzo[b][1,4]oxazin-6-ol (7): A solution of 6 (2.2 g, 13.3 mmol) in anhydrous THF (40 mL) was stirred in an ice bath under N for 30 min. Borane tetrahydrofuran complex solution (1 M, 40 mL) was added to the above solution over 30 min using a syringe pump, maintaining the solution temperature below 5 °C. The resulting reaction mixture was allowed to warm slowly to room temperature while still in the ice bath. After 24 h, the solution was placed back in the ice bath, and excess borane reagent was quenched by careful addition of MeOH until no more gas was evolved. The solvent was evaporated under reduced pressure, and the residue was purified by flash column chromatography on silica gel using ErOAc / hexane as eluent to give 7 (1.91 g, 95%).

[0125] 1-(6-Hydroxy-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)ethan-1-one (8): Compound 7 (1.00 g, 6.62 mmol) was suspended in 10 mL of DI water, to which acetic anhydride (2.5 mL, 26.5 mmol) was added dropwise. The reaction mixture was placed in an ultrasonic bath for 1 minute and then stirred in a water bath (50 °C) for 10 minutes. The resulting solution was stirred at room temperature overnight. The solid was then collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 8 (1.21 g, 95%) as a white solid, which was used in the next step without further purification.

[0126] 4-Ethyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ol (9): A solution of 8 (900 mg, 10.0 mmol) in anhydrous THF (14 mL) was stirred in an ice bath under N for 30 min. Borane tetrahydrofuran complex solution (1 M, 14 mL) was added to the solution over 30 min using a syringe pump, maintaining the solution temperature below 5 °C. The resulting reaction mixture was allowed to warm slowly to room temperature while remaining in the ice bath. After 24 h, the solution was placed back in the ice bath, and excess borane reagent was quenched by careful addition of MeOH until no more gas was evolved. The solvent was evaporated under reduced pressure, and the residue was purified by flash column chromatography on silica gel using DCM / hexane as eluent to give 9 (756 mg, 91%) as a brown oil.

[0127] N-(4-Ethyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)-N-methylmethanaminium (LGW11-98): Compound 9 (40 mg, 0.22 mmol) was dissolved in a solution of i-PrOH / HO (9 / 1, 3 mL) at 80 °C for 30 min. Compound 2 (73 mg, 0.22 mmol) was added in five portions over 15 min. The reaction mixture was then treated with HClO (70%, 20 μL). The resulting solution was stirred overnight. The dark blue solution was evaporated under reduced pressure, and the residue was purified by flash column chromatography on silica gel using a mobile phase of CHCl containing 0.5% formic acid and MeOH (linear gradient, 2–15% MeOH in CHCl). Fractions containing the product were pooled and evaporated to give LGW11-98 (26 mg, 38%) as a dark blue solid. MS(ESI):C 18 H 20 N3O2[M] + Calculated value 310.1550; measured value 310.1563.

[0128] TIFF0007781065000048.tif46128 Scheme : Synthetic route to LGW13-79. Reagents and conditions: a) MeI, NaH, THF, 0 °C to room temperature; b) 2M HCl, NaNO2, 0 °C; ii) K2CO3, 0 °C; c) Pd(OAc)2, velcade base, LiHMDS, azetidine, toluene, 80 °C; d) Compound 12, HClO4, 90% i-PrOH, 80 °C.

[0129] N,N-Diethyl-3-methoxyaniline (11): Compound 10 (5.00 g, 30.3 mmol) was dissolved in anhydrous THF (50 mL) under N2 and cooled in an ice bath for 30 min. NaH (60%, 3.63 g, 90.8 mmol) was added to the solution in three portions over 10 min, maintaining the temperature below 5 °C. After 10 min, MeI (7.54 mL, 121 mmol) was added to the reaction mixture in one portion. The resulting suspension was allowed to warm slowly to room temperature and stirred overnight. Upon completion, DI water was added to the reaction mixture to quench excess NaH. The organic solvent was removed under reduced pressure, and the residue was extracted with DCM (3 × 100 mL). The combined organic layers were rinsed with brine, dried over anhydrous Na2SO4, and the solvent was removed using a rotary evaporator. The residue was purified by flash column chromatography on silica gel with DCM / hexane as eluent to give compound 11 (4.70 g, 88%) as a clear oil.

[0130] N,N-Diethyl-3-methoxy-4-nitrosoaniline (12): Compound 11 (1.08 g, 6.02 mmol) was dissolved in ice-cold 2 M HCl solution (15 mL). To the above solution, NaNO (457 mg, 6.63 mmol) was added portionwise over 1 h, while maintaining the solution temperature below 5 °C so that brown NO vapors were not observed. The reaction mixture was stirred for an additional 2 h. The solution was carefully basified with solid KCO until the pH value of the solution was higher than 8. The precipitate was then filtered through a Buchner funnel and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 12 (1.05 g, 84%) as a green solid, which was used in the next step without further purification.

[0131] 3-(Azetidin-1-yl)phenol (14): Grimm et al. 7Compound 14 was synthesized according to a slightly modified protocol published by

[1999] . An oven-dried flask was charged with Pd(OAc)2 (52 mg, 0.231 mmol). The flask was sealed, evacuated under vacuum, and refilled with N2 five times. Toluene (40 mL) was then added. A solution of compound 13 (2.00 g, 11.6 mmol) in toluene (10 mL), a solution of 2,8,9-triisobutyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane (159 mg, 0.463 mmol) in toluene (10 mL), and a LiHMDS solution (1.3 M, 20 mL, 26 mmol) were then added sequentially. After the addition of azetidine (792 mg, 13.9 mmol), the reaction was stirred at 80 °C overnight. It was then cooled to room temperature, deposited onto Celite, and concentrated to dryness. Purification by silica gel flash chromatography using a mobile phase of EtOAc and hexanes gave compound 14 (1.38 g, 80%) as an off-white solid.

[0132] 1-(7-(Diethylamino)-3H-phenoxazin-3-ylidene)azetidin-1-ium (LGW13-79): Compound 14 (40 mg, 0.268 mmol) was dissolved in a solution of i-PrOH / HO (9 / 1, 4 mL) at 80 °C for 30 min. Compound 12 (56 mg, 0.268 mmol) was added in five portions over 15 min. The reaction mixture was then treated with HClO (70%, 20 μL). The resulting solution was stirred overnight. The dark blue solution was then cooled to room temperature and evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel using a mobile phase of CHCl containing 0.5% formic acid and MeOH (linear gradient, 2 to 15% MeOH in CHCl). Fractions containing the product were pooled and evaporated to give LGW13-79 (25 mg, 30%) as a dark blue solid. MS (ESI): C 19 H 22 N3O[M] + Calculated value 308.1757; measured value 308.1763.

[0133] TIFF0007781065000049.tif44128 Scheme: Synthetic route to LGW14-42. Reagents and conditions: a) chloroacetic acid chloride, K2CO3, MeCN, 80 °C; b) BH3-THF, THF, 0 °C to room temperature; c) EtI, Na2CO3, MeCN, 80 °C; d) i) 2M HCl, p-nitrobenzenediazonium tetrafluoroborate, 0 °C; ii) K2CO3, 0 °C; e) compound 14, PPSE, CF3CH2OH, 80 °C.

[0134] 6-Methoxy-2H-benzo[b][1,4]oxazin-3(4H)-one (16): Zhang et al. 8 Compound 16 was synthesized according to a slightly modified protocol reported by

[14] . Compound 15 (2.00 g, 14.4 mmol) was dissolved in anhydrous MeCN (20 mL) under a N atmosphere, and 2-chloroacetyl chloride (1.37 mL, 17.3 mmol) was added dropwise to the solution. After KCO (4.97 g, 25.9 mmol) was added, the reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, diluted with DCM, and filtered through Celite. The solvent was removed in vacuo, and the residue was purified by silica gel flash chromatography using a mobile phase of EtOAc and hexane to give compound 16 (2.21 g, 86%) as a brown solid.

[0135] 6-Methoxy-3,4-dihydro-2H-benzo[b][1,4]oxazine (17): A solution of compound 16 (2.00 g, 11.2 mmol) in anhydrous THF (30 mL) was stirred in an ice bath under N for 30 min. Borane tetrahydrofuran complex solution (1 M, 30 mL) was added dropwise to the above solution over 30 min using a syringe pump, maintaining the solution temperature below 5 °C. The resulting reaction mixture was allowed to slowly warm to room temperature while stirring in the ice bath. After 24 h, the solution was placed back in the ice bath, and excess borane reagent was quenched by careful addition of MeOH until no gas evolution occurred. The solvent was evaporated under reduced pressure, and the residue was purified by flash column chromatography on silica gel using DCM / hexane as eluent to give compound 17 (1.62 g, 88%) as a pale pink solid.

[0136] 4-Ethyl-6-methoxy-3,4-dihydro-2H-benzo[b][1,4]oxazine (18): To a suspension of compound 17 (1.00 g, 6.05 mmol) and NaCO (1.28 g, 12.1 mmol) in anhydrous MeCN (10 mL) under N was added EtI (0.501 mL, 6.17 mmol) at room temperature. The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, diluted with DCM, and filtered through Celite. The solvent was removed in vacuo, and the residue was purified by silica gel flash chromatography on silica gel using DCM / hexane as eluent to give compound 18 (1.01 g, 86%) as a light brown oil.

[0137] (E)-4-Ethyl-6-methoxy-7-((4-nitrophenyl)diazenyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine (19): Compound 18 (400 mg, 2.07 mmol) was dissolved in MeOH (1 mL). The solution was cooled in an ice bath and then treated with HCl (2 M, 10 mL). After 15 min, p-nitrobenzenediazonium tetrafluoroborate (515 mg, 2.17 mmol) was added to the solution in three portions over an additional 15 min, followed by stirring at 0 °C for 1 h. During this time, the color of the reaction mixture changed from orange to dark red. After 2 h, the solution was carefully neutralized with solid KCO until the pH value of the solution exceeded 7. The precipitate was collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 19 (537 mg, 76%) as a green solid, which was used in the next step without further purification.

[0138] 1-(4-Ethyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)azetidin-1-ium (LGW14-42): Compounds 14 (30 mg, 0.201 mmol) and 19 (69 mg, 0.201 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 20 N3O2[M] + Calculated value 322.1550; measured value 322.1584.

[0139] TIFF0007781065000050.tif20147 Scheme Synthesis of LGW14-45. Reagents and conditions: a) MeI, Na2CO3, MeCN, 80°C; b) i) 2M HCl, p-nitrobenzenediazonium tetrafluoroborate, 0°C; ii) K2CO3, 0°C; c) Compound 1, PPSE, CF3CH2OH, 80°C.

[0140] 6-Methoxy-4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazine (20): To a suspension of compound 17 (1.00 g, 6.05 mmol) and NaCO (1.28 g, 12.1 mmol) in anhydrous MeCN (10 mL) under N was added MeI (400 μL, 6.36 mmol) at room temperature. The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, diluted with DCM, and filtered through Celite. The solvent was removed in vacuo, and the residue was purified by silica gel flash chromatography on silica gel using DCM / hexane as eluent to give compound 20 (0.814 g, 75%) as a burgundy oil.

[0141] (E)-6-Methoxy-4-methyl-7-((4-nitrophenyl)diazenyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine (21): Compound 20 (400 mg, 2.23 mmol) was dissolved in MeOH (1 mL). The solution was cooled in an ice bath and then treated with HCl (2 M, 10 mL). After 15 min, p-nitrobenzenediazonium tetrafluoroborate (555 mg, 2.34 mmol) was added to the solution in three portions over an additional 15 min, followed by stirring at 0 °C for 1 h. During this time, the color of the reaction mixture changed from orange to dark red. After 2 h, the solution was carefully neutralized with solid KCO until the pH value of the solution exceeded 7. The precipitate was collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 21 (693 mg, 95%) as a dark red solid, which was used in the next step without further purification.

[0142] N-Methyl-N-(4-methyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)methanaminium (LGW14-45): Compound 1 (30 mg, 0.219 mmol) and 21 (72 mg, 0.219 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 17 H 18 N3O2[M] + Calculated value 296.1394; measured value 296.1441.

[0143] TIFF0007781065000051.tif23130 Scheme : Synthetic route to LGW14-46. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0144] N-Ethyl-N-(4-methyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)ethanaminium (LGW14-46): Compounds 10 (30 mg, 0.182 mmol) and 21 (60 mg, 0.182 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 22 N3O2[M] + Calculated value 324.1707; measured value 324.1746.

[0145] TIFF0007781065000052.tif23128 Scheme : Synthetic route to LGW14-47. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0146] 1-(4-Methyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)azetidin-1-ium (LGW14-47): Compounds 14 (30 mg, 0.201 mmol) and 21 (66 mg, 0.201 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 18 N3O2[M] + Calculated value 308.1394; measured value 308.1436.

[0147] TIFF0007781065000053.tif50150 Scheme: Synthetic route to LGW14-49. Reagents and conditions: a) Ac2O, H2O, 50 °C to room temperature; b) BH3-THF, THF, 0 °C to room temperature; c) MeI, Na2CO3, MeCN, 80 °C; d) i) 2M HCl, p-nitrobenzenediazonium tetrafluoroborate, 0 °C; ii) K2CO3, 0 °C; e) compound 10, PPSE, CF3CH2OH, 80 °C.

[0148] N-(3-Methoxyphenyl)acetamide (23): Compound 22 (2.00 g, 16.2 mmol) was suspended in 20 mL of DI water, to which acetic anhydride (4.61 mL, 48.7 mmol) was added dropwise. The reaction mixture was placed in an ultrasonic bath for 1 minute and then stirred in a warm water bath (50 °C) for 10 minutes. The resulting solution was stirred at room temperature overnight. The solid product was collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 23 (2.37 g, 88%) as an off-white solid, which was used in the next step without further purification.

[0149] N-Ethyl-3-methoxyaniline (24): A solution of compound 23 (2.00 g, 12.1 mmol) in anhydrous THF (30 mL) was stirred in an ice bath under N for 30 min. Borane tetrahydrofuran complex solution (1 M, 30 mL) was added dropwise to the above solution over 30 min using a syringe pump, maintaining the solution temperature below 5 °C. The resulting reaction mixture was allowed to slowly warm to room temperature while stirring in the ice bath. After 24 h, the solution was placed back in the ice bath, and excess borane reagent was quenched by careful addition of MeOH until no more gas was evolved. The solvent was evaporated under reduced pressure, and the residue was purified by flash column chromatography on silica gel using DCM / hexane as eluent to give compound 24 (1.47 g, 80%) as an oil.

[0150] N-Ethyl-3-methoxy-N-methylaniline (25): To a suspension of compound 24 (1.00 g, 6.61 mmol) and NaCO (1.05 g, 9.92 mmol) in anhydrous MeCN (10 mL) under N was added MeI (424 μL, 6.75 mmol) at room temperature. The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, diluted with DCM, and filtered through Celite. The solvent was removed in vacuo, and the residue was purified by silica gel flash chromatography on silica gel (25 g) using DCM / hexane as eluent to give compound 25 (917 mg, 84%) as a pale yellow solid.

[0151] (E)-N-Ethyl-3-methoxy-N-methyl-4-((4-nitrophenyl)diazenyl)aniline (26): Compound 25 (400 mg, 2.42 mmol) was dissolved in MeOH (1 mL). The solution was cooled in an ice bath and then treated with HCl (2 M, 10 mL). After 15 min, p-nitrobenzenediazonium tetrafluoroborate (602 mg, 2.54 mmol) was added to the solution in three portions over an additional 15 min, followed by stirring at 0 °C for 1 h. During this time, the color of the reaction mixture changed from orange to dark red. After 2 h, the solution was carefully neutralized with solid K2CO3 until the pH value of the solution exceeded 7. The precipitate was collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 26 (714 mg, 94%) as a dark red solid, which was used in the next step without further purification.

[0152] N-Ethyl-N-(7-(ethyl(methyl)amino)-3H-phenoxazin-3-ylidene)ethanaminium (LGW14-49): Compounds 10 (30 mg, 0.182 mmol) and 26 (57 mg, 0.182 mmol) were dissolved in trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 24 N3O[M] + Calculated value 310.1914; measured value 310.1943.

[0153] TIFF0007781065000054.tif23130 Scheme :Synthetic route to LGW14-50. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0154] N-(7-(ethyl(methyl)amino)-3H-phenoxazin-3-ylidene)-N-methylmethanaminium (LGW14-50): Compounds 1 (30 mg, 0.219 mmol) and 26 (69 mg, 0.219 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 17 H 20 N3O[M] + Calculated value 282.1601; measured value 282.1626.

[0155] TIFF0007781065000055.tif21128 Scheme: Synthetic route to LGW14-51. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0156] (E)-N-(7-(azetidin-1-yl)-3H-phenoxazin-3-ylidene)-N-methylethanaminium (LGW14-51): Compounds 14 (30 mg, 0.201 mmol) and 26 (63 mg, 0.201 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 20 N3O[M] + Calculated value 294.1601; measured value 294.1634.

[0157] TIFF0007781065000056.tif49128 Scheme Synthetic route to LGW14-53. Reagents and conditions: a) Pd2(dba)3, Xphos, Cs2CO3, azetidine, dioxane, 100 °C; b) i) 2M HCl, p-nitrobenzenediazonium tetrafluoroborate, 0 °C; ii) K2CO3, 0 °C; c) compound 14, PPSE, CF3CH2OH, 80 °C.

[0158] 1-(3-Methoxyphenyl)azetidine (28): A heated, dried flask was charged with a magnetic stir bar, compound 27 (2.00 g, 10.7 mmol), Pd(dba) (979 mg, 1.07 mmol), Xphos (1.53 g, 3.21 mmol), and CsCO (4.88 g, 14.97 mmol). The flask was sealed, evacuated under vacuum, and refilled with N five times before delivering azetidine (800 μL, 11.8 mmol) and anhydrous dioxane (20 mL) via syringe. The reaction was heated to 100 °C and stirred for 6 h, then cooled to room temperature and diluted with DCM (20 mL). The solids were removed via filtration through Celite, and the filtrate was then deposited onto Celite and concentrated to dryness. Purification by silica gel flash chromatography using a mobile phase of EtOAc and hexanes gave compound 28 (1.58 g, 91%) as a yellow-orange solid.

[0159] (E)-1-(3-Methoxy-4-((4-nitrophenyl)diazenyl)phenyl)azetidine (29): Compound 28 (400 mg, 2.45 mmol) was dissolved in MeOH (1 mL). The solution was cooled in an ice bath and then treated with HCl (2 M, 10 mL). After 15 min, p-nitrobenzenediazonium tetrafluoroborate (639 mg, 2.70 mmol) was added to the solution in three portions over an additional 15 min, followed by stirring at 0 °C for 1 h. During this time, the color of the reaction mixture changed from orange to dark red. After 2 h, the solution was carefully neutralized with solid K2CO3 until the pH value of the solution exceeded 7. The precipitate was collected via vacuum filtration and washed with small portions of DI water. The product was left in the funnel and air-dried overnight to give compound 29 (630 mg, 82%) as a black solid, which was used in the next step without further purification.

[0160] 1-(7-(Azetidin-1-yl)-3H-phenoxazin-3-ylidene)azetidin-1-ium (LGW14-53): Compounds 14 (29 mg, 0.192 mmol) and 29 (60 mg, 0.192 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 18 N3O[M] + Calculated value 292.1444; measured value 292.1481.

[0161] TIFF0007781065000057.tif19128 Scheme : Synthetic route to LGW14-57. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0162] N-(7-(azetidin-1-yl)-3H-phenoxazin-3-ylidene)-N-methylmethanaminium (LGW14-57): Compounds 14 (30 mg, 0.201 mmol) and 2 (34 mg, 0.201 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 17 H 18 N3O[M] + Calculated value 280.1444; measured value 280.1491.

[0163] TIFF0007781065000058.tif43128 Scheme: Synthetic route to LGW14-61. Reagents and conditions: a) i) 1,4-dichlorobutane, toluene, reflux; ii) Et3N, Na2CO3, reflux; b) 6M HCl, NaNO2, 0°C; c) Compound 1, PPSE, CF3CH2OH, 80°C.

[0164] 3-(Pyrrolidin-1-yl)phenol (31): Ghashang 9 Following the protocol reported by

[1999] , 1,4-dichlorobutane (5.52 mL, 50.4 mmol) was added to a suspension of compound 30 (5.00 g, 45.82 mmol) in anhydrous toluene. The reaction mixture was refluxed for 24 h and then cooled to room temperature. Upon cooling, EtN (9.58 mL, 68.7 mmol) and NaCO (4.86 g, 45.8 mmol) in 10 mL of DI water were added to the reaction flask. The resulting reaction mixture was refluxed for an additional 24 h. Upon completion of the reaction, the organic solvent was removed under reduced pressure, and the aqueous phase was extracted with DCM (3 × 100 mL). The combined organic layers were rinsed with brine, dried over anhydrous NaSO, and the solvent was removed using a rotary evaporator. The residue was purified by flash column chromatography on silica gel using DCM / hexane as the eluent to give compound 31 (5.37 g, 72%) as a light gray solid.

[0165] 2-Nitroso-5-(pyrrolidin-1-yl)phenol (32): Compound 31 (400 mg, 2.45 mmol) was dissolved in ice-cold 6 M HCl solution (4 mL). NaNO (178 mg, 2.57 mmol) was added portionwise over 1 h to the solution, maintaining the solution temperature below 5 °C so that brown NO vapors were not observed. The reaction mixture was stirred for an additional 2 h. After this time, the precipitate was filtered through a Buchner funnel and washed with small portions of ice-cold 2 M HCl solution. The product was left in the funnel and air-dried overnight to give compound 32 (0.403 g, 86%) as a bright yellow solid, which was used in the next step without further purification.

[0166] 1-(7-(Dimethylamino)-3H-phenoxazin-3-ylidene)pyrrolidin-1-ium (LGW14-61): Compounds 1 (30 mg, 0.219 mmol) and 32 (42 mg, 0.219 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 20 N3O[M] + Calculated value 294.1601; measured value 294.1622.

[0167] TIFF0007781065000059.tif23129 Scheme : Synthetic route to LGW14-63. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0168] 1-(4-Methyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)pyrrolidin-1-ium (LGW14-63): Compounds 31 (30 mg, 0.184 mmol) and 21 (61 mg, 0.184 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 20 N3O2[M] + Calculated value 322.1550; measured value 322.1591.

[0169] TIFF0007781065000060.tif22136 Scheme: Synthetic route to LGW14-72. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0170] 1-(7-(Ethyl(methyl)amino)-3H-phenoxazin-3-ylidene)pyrrolidin-1-ium (LGW14-72): Compounds 31 (30 mg, 0.184 mmol) and 26 (58 mg, 0.184 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 22 N3O[M] + Calculated value 308.1757; measured value 308.1783.

[0171] TIFF0007781065000061.tif24130 Scheme : Synthetic route to LGW14-76. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0172] 1-(4-Ethyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)pyrrolidin-1-ium (LGW14-76): Compounds 31 (30 mg, 0.184 mmol) and 19 (63 mg, 0.184 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 20 H 22 N3O2[M] + Calculated value 336.1707; measured value 336.1753.

[0173] TIFF0007781065000062.tif19128 Scheme : Synthetic route to LGW14-83. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0174] 1-(7-(pyrrolidin-1-yl)-3H-phenoxazin-3-ylidene)azetidin-1-ium (LGW14-83): Compounds 14 (30 mg, 0.201 mmol) and 32 (39 mg, 0.201 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 20 N3O[M] + Calculated value 306.1601; measured value 306.1627.

[0175] TIFF0007781065000063.tif18128 Scheme : Synthetic route to LGW14-88. Reagents and conditions: a) 1M BBr3, DCM, 0 °C to room temperature; b) compound 26, PPSE, CF3CH2OH, 80 °C.

[0176] 4-Methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ol (33): Compound 20 (100 mg, 0.558 mmol) was dissolved in anhydrous DCM (5 mL) under N and cooled in an ice bath. To the above solution was added BBr (1 M in DCM, 2 mL, 1.95 mmol) dropwise. The reaction mixture was allowed to warm slowly to room temperature and stirred overnight. The reaction flask was placed in an ice bath, and after sufficient cooling time, water was carefully added to the reaction mixture to quench excess BBr and neutralize with NaCO to pH 7. The aqueous phase was then extracted with EtOAc (4 × 10 mL). The combined organics were dried over anhydrous NaSO, filtered, and concentrated in vacuo. Flash chromatography on silica gel afforded compound 33 (61 mg, 66%) as a burgundy oil.

[0177] (E)-N-Methyl-N-(4-methyl-3,4-dihydro-[1,4]oxazino[2,3-b]phenoxazin-8(2H)-ylidene)ethanaminium (LGW14-88): Compounds 33 (10 mg, 0.061 mmol) and 26 (19 mg, 0.061 mmol) were dissolved in a solution of trifluoroethanol (1 mL) containing trimethylsilyl polyphosphate (10 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 20 N3O2[M] + Calculated value 310.1550; measured value 310.1578.

[0178] TIFF0007781065000064.tif18128 Scheme : Synthetic route to LGW14-90. Reagents and conditions: a) 1M BBr3, DCM, 0 °C to room temperature; b) compound 26, PPSE, CF3CH2OH, 80 °C.

[0179] 3-(Ethyl(methyl)amino)phenol (34): Compound 25 (100 mg, 0.605 mmol) was dissolved in anhydrous DCM (5 mL) under N2 and cooled in an ice bath. To the above solution was added BBr3 (1 M in DCM, 2.2 mL, 2.12 mmol) dropwise. The reaction mixture was allowed to warm slowly to room temperature and stirred overnight. The reaction flask was placed in an ice bath, and after sufficient cooling time, water was carefully added to the reaction mixture to quench excess BBr3 and neutralize with Na2CO3 to pH 7. The aqueous phase was then extracted with EtOAc (4 × 10 mL). The combined organics were dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. Flash chromatography on silica gel afforded compound 34 (75 mg, 82%) as a clear oil.

[0180] (E)-N-(7-(ethyl(methyl)amino)-3H-phenoxazin-3-ylidene)-N-methylethanaminium (LGW14-90): Compounds 34 (30 mg, 0.198 mmol) and 26 (62 mg, 0.198 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 22 N3O[M] + Calculated value 296.1757; measured value 296.1800.

[0181] TIFF0007781065000065.tif24128 Scheme : Synthetic route to LGW14-92. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0182] 4,8-Dimethyl-3,8,9,10-tetrahydro-2H-bis([1,4]oxazino)[2,3-b:3',2'-i]phenoxazin-4-ium (LGW14-92): Compounds 33 (10 mg, 0.061 mmol) and 21 (20 mg, 0.061 mmol) were dissolved in a solution of trifluoroethanol (1 mL) containing trimethylsilyl polyphosphate (10 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 18 H 18 N3O3[M] + Calculated value 324.1343; measured value 324.1361.

[0183] TIFF0007781065000066.tif24128 Scheme :Synthetic route to LGW14-95. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0184] 4-Ethyl-8-methyl-3,8,9,10-tetrahydro-2H-bis([1,4]oxazino)[2,3-b:3',2'-i]phenoxazin-4-ium (LGW14-95): Compounds 33 (10 mg, 0.061 mmol) and 19 (21 mg, 0.061 mmol) were dissolved in a solution of trifluoroethanol (1 mL) containing trimethylsilyl polyphosphate (10 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 20 N3O3[M] + Calculated value 338.1499; measured value 338.1529.

[0185] TIFF0007781065000067.tif24130 Scheme :Synthetic route to LGW14-98. Reagents and conditions: a) PPSE, CF3CH2OH, 80°C.

[0186] 4-Ethyl-8-(ethyl(methyl)amino)-2,3-dihydro-[1,4]oxazino[2,3-b]phenoxazin-4-ium (LGW14-98): Compounds 34 (30 mg, 0.198 mmol) and 19 (68 mg, 0.198 mmol) were dissolved in a solution of trifluoroethanol (3 mL) containing trimethylsilyl polyphosphate (30 μL). The reaction mixture was heated to 80 °C and stirred overnight. It was then cooled to room temperature, and the solvent was removed in vacuo. The residue was purified by silica gel flash chromatography using a mobile phase of CHCl3 containing 1% formic acid and MeOH (gradient, 2 to 15% MeOH in CHCl3). MS (ESI): C 19 H 22 N3O2[M] + Calculated value 324.1707; measured value 324.1722.

[0187] HPLC-MS characterization of the oxazine derivative library. Using HPLC-MS, the purity of each oxazine derivative was quantified via area under the curve (AUC) analysis of absorbance at 254 nm (left) and mass-to-charge ratio (m / z) in positive ion mode (right). Samples (5 μL) were injected onto a C18 column (Poroshell 120, 2.1 × 50 mm, 2.7 μm) and eluted at 0.4 mL / min with a solvent system of A (HO, 0.1% formic acid) and B (acetonitrile, 0.1% formic acid), ranging from A / B = 95 / 5 to 5 / 95 for 6 min, followed by a 2-min hold at A / B = 5 / 95. Ions were detected in positive ion mode by setting the capillary voltage at 4 kV and the gas temperature at 350 °C. The purity was determined to be 97% for LGW-76 and >99% for LGW-13-79, LGW14-42, LGW14-47, LGW14-51, LGW14-53, and LGW14-83. TIFF0007781065000068.tif64166

[0188] Figures 1A-1F show the normalized absorption and fluorescence emission spectra of the oxazine derivatives in PBS. Compounds LGW14-42 and LGW14-27 both absorb and emit in the NIR, while the rest only emit in the NIR. LGW14-42 is the most red-shifted fluorophore among the seven candidate compounds screened.

[0189] Figure 2 - In vivo direct administration nerve specificity screening. A. Representative photographs and fluorescence images of NIR oxazine derivatives after direct application (125 μM in co-solvent formulation) to exposed brachial plexus and sciatic nerves. All images represent data collected for n=6 nerve sites per fluorophore. B. Average nerve (white), muscle (black), and fat (gray) tissue intensity per second quantified compared to the unstained control group. C. Quantified nerve SBR was calculated for comparison of the screened oxazine derivatives with the unstained control group. All quantified data are expressed as mean ± standard deviation.

[0190] Figure 3 - Pharmacokinetic study of NIR neurospecific candidate LGW03-76. A. Representative photographs and fluorescence images of NIR neurospecific candidate LGW03-76 after systemic administration at 0.5, 1, 2, and 4 hours. B. Average nerve (white), muscle (black), and fat (gray) tissue intensity per second quantified and compared to control tissue autofluorescence. C. Quantified nerve SBR was calculated for comparison of LGW03-76 to control tissue autofluorescence. All quantified data are expressed as mean ± standard deviation.

[0191] Figure 4 - Pharmacokinetic study of NIR neurospecific candidate LGW13-79. A. Representative photographs and fluorescence images of NIR neurospecific candidate LGW13-79 after systemic administration at 0.5, 1, 2, and 4 hours. B. Average nerve (white), muscle (black), and fat (gray) tissue intensity per second quantified and compared to control tissue autofluorescence. C. Quantified nerve SBR was calculated for comparison of LGW13-79 to control tissue autofluorescence. All quantified data are expressed as mean ± standard deviation.

[0192] Figure 5 - Pharmacokinetic study of NIR neurospecific candidate LGW14-42. A. Representative photographs and fluorescence images of NIR neurospecific candidate LGW14-42 after systemic administration at 0.5, 1, 2, and 4 hours. B. Average nerve (white), muscle (black), and fat (gray) tissue intensity per second quantified and compared to control tissue autofluorescence. C. Quantified nerve SBR was calculated for comparison of LGW14-42 to control tissue autofluorescence. All quantified data are expressed as mean ± standard deviation.

[0193] Experimental LogD Measurement. Each screening candidate was dissolved in DMSO at a concentration of 10 mM. A sample (2 μL) of the stock solution was added to a 1 mL mixture of 1-octanol and PBS buffer (equal volumes). The solution was then vortexed at room temperature for 30 minutes and then centrifuged at 13,000 rpm for 5 minutes. The PBS buffer and 1-octanol layers were separated, and the absorbance was measured using a SpectraMax M5 spectrometer equipped with a microplate reader (Molecular Devices, Sunnyvale, CA). The sample concentration in each phase was then calculated using a Beer's Law plot of absorbance versus concentration. The experimental LogD value for each screening candidate was calculated using the following formula: TIFF0007781065000069.tif10128

[0194] References TIFF0007781065000070.tif216165TIFF0007781065000071.tif114165

Claims

1. Formula (I): Compound of: During the ceremony, R 2 and R 3 are taken together to form a fused ring of formula (II): or R 2 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or is a moiety selected from the group R 3 is hydrogen; R 1 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group R 4 and R 5 together with the nitrogen atoms to which they are attached, forming a ring selected from the group R 6 is hydrogen; However, R 4 and R 5 together with the nitrogen atom to which they are attached form a ring and R 3 If is H, then R 1 and R 2 may be taken together with the nitrogen atom to which they are attached to form a pyrrolidinyl ring; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and provided that the sum of n2+n2 is 10 or less; provided that the sum of n2+n3 is 10 or less; provided that the sum of n2+n4 is 10 or less; provided that the sum of n3+n4 is 10 or less; However, R 4 and R 5 together with the nitrogen atom to which they are attached form a ring If R 1 and R 2 are not both methyl, and R 1 and R 2 are not both ethyl, and R 1 and R 2 are not n-propyl, and R 1 and R 2 are not both n-butyl, and R 1 and R 2 are not both n-pentyl.

2. Formula (IV): and During the ceremony, R 2 and R 3 are taken together to form a fused ring of formula (V): or R 2 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or is a moiety selected from the group R 3 is hydrogen; R 1 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group provided that n is 1 and R 3 If is H, then R 1 and R 2 may be taken together with the nitrogen atom to which they are attached to form a pyrrolidinyl ring; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and provided that the sum of n2+n2 is 10 or less; provided that the sum of n2+n3 is 10 or less; provided that the sum of n2+n4 is 10 or less; provided that the sum of n3+n4 is 10 or less; and However, when n is 2, R 1 and R 2 are not both methyl, and R 1 and R 2 are not both ethyl, and R 1 and R 2 are not n-propyl, and R 1 and R 2 are not both n-butyl, and R 1 and R 2 are not both n-pentyl, The compound of claim 1.

3. Formula (VII): and During the ceremony, R 2 and R 3 are taken together to form a fused ring of formula (VIIIb): or R 2 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or is a moiety selected from the group R 3 is hydrogen; R 1 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and provided that the sum of n2+n2 is 10 or less; provided that the sum of n2+n3 is 10 or less; provided that the sum of n2+n4 is 10 or less; However, the sum of n3 + n4 is 10 or less. The compound of claim 1.

4. Formula (VI): and During the ceremony, R 2 and R 3 are taken together to form a fused ring of formula (Va): or R 2 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or is a moiety selected from the group R 3 is hydrogen; R 1 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group However, R 3 If is H, then R 1 and R 2 may be taken together with the nitrogen atom to which they are attached to form a pyrrolidinyl ring; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and provided that the sum of n2+n2 is 10 or less; provided that the sum of n2+n3 is 10 or less; provided that the sum of n2+n4 is 10 or less; and However, the sum of n3 + n4 is 10 or less. The compound of claim 1.

5. R 1 Is linear or branched C 1 ~C 3 2. The compound of claim 1, wherein the alkyl is selected from the group:

6. Formula (V): and During the ceremony, R 1 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n is an integer selected from the group of 1 and 2; n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; However, the sum of n2 + n4 is 10 or less. The compound of claim 1.

7. formula:

7. The compound of claim 6, having the formula:

8. formula:

7. The compound of claim 6, having the formula:

9. Formula (III): and During the ceremony, R 1 is -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group R 4 is C 1 ~C 6 is alkyl; X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; and n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; However, the sum of n2 and n4 is 10 or less. compound.

10. the below described: A compound selected from the group consisting of:

11. The compound of claim 1, selected from the group consisting of:

12. 12. An imaging composition comprising an effective amount of a compound of any one of claims 1 to 11 and a pharmaceutically or physiologically acceptable carrier.

13. A pharmaceutical composition for detecting nerves in a tissue or organ, comprising: The composition comprises an effective amount of a compound according to any one of claims 1 to 11, The composition can be prepared by the following steps: a) administering the composition to the tissue or organ to form a stained tissue or a stained organ; and b) imaging said stained tissue or stained organ, thereby detecting nerves intraoperatively in said stained tissue or stained organ. The pharmaceutical composition used according to the method of claim 1.

14. A pharmaceutical composition for detecting nerves in a tissue or organ, the composition comprising a compound represented by the following formula (II): (In the formula, R 1 is a linear or branched C 1 ~C 6 Alkyl; -(CH 2 ) n1 -SO 3 - , -(CH 2 ) n1 -N + (CH 3 ) 3 , -CH 2 -CH 2 -OX 1 , -CH 2 -CH 2 -O-[CH 2 -CH 2 -O] n2 -X 1 , -CH 2 -CH 2 -CH 2 -OX 1 , and -CH 2 -CH 2 -CH 2 -O-[CH 2 -CH 2 -CH 2 -O] n3 -X 1 or selected from the group is a moiety selected from the group X in each case 1 independently, C 1 ~C 6 Straight or branched alkyl, C 1 ~C 6 Straight or branched alkenyl, C 1 ~C 6 Linear or branched alkynyl, and -Si(C 1 ~C 4 alkyl) 3 Selected from: n1, at each occurrence, is an integer independently selected from the group of 1, 2, 3, and 4; n2, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n3, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; n4, at each occurrence, is an integer independently selected from the group of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10; R 4 and R 5 are each independently C 1 ~C 6 alkyl; R 6 is hydrogen, provided that the sum of n2+n2 is 10 or less; provided that the sum of n2+n3 is 10 or less; provided that the sum of n2+n4 is 10 or less; provided that the sum of n3+n4 is 10 or less; However, R 1 is methyl and R 4 is ethyl, R 5 is not ethyl) The compound includes a compound represented by The composition can be prepared by the following steps: a) administering the composition to the tissue or organ to form a stained tissue or a stained organ; and b) imaging said stained tissue or stained organ, thereby detecting nerves intraoperatively in said stained tissue or stained organ. The pharmaceutical composition used according to the method of claim 1.

15. R 1 Is linear or branched C 1 ~C 3 15. The pharmaceutical composition of claim 14, wherein the alkyl group is selected from the group consisting of:

16. A pharmaceutical composition for detecting nerves in a tissue or organ, the composition comprising: and a compound selected from the group consisting of: The composition can be prepared by the following steps: a) administering the composition to the tissue or organ to form a stained tissue or a stained organ; and b) imaging said stained tissue or stained organ, thereby detecting nerves intraoperatively in said stained tissue or stained organ. The pharmaceutical composition used according to the method of claim 1.

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