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Charged ion channel blockers and methods for use

a technology of ion channel blockers and ion channel blockers, which is applied in the field of charged ion channel blockers and methods for use, can solve the problems of non-productive dry cough, inappropriate cough reflexes, and unwanted or deleterious effects of local anesthetics, and achieve the effects of reducing the risk of infection, and reducing the effect of local anesthetic us

Active Publication Date: 2020-09-17
NOCION THERAPEUTICS INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides compounds that can be used to treat or prevent pain, itch, and neurogenic inflammation. These compounds have a specific formula and can be used with different anions, such as pharmaceutically acceptable anions like halide ions, sulfonate ions, or carboxylate ions. The compounds can be formulated into suitable dosage forms for systemic or topical use. By using these compounds, it is possible to provide new treatments for pain, itch, and neurogenic inflammation.

Problems solved by technology

Thus, while the goal of topical or regional anesthesia is to block transmission of signals in nociceptors to prevent pain, administration of local anesthetics also produces unwanted or deleterious effects such as general numbness from block of low threshold pressure and touch receptors, motor deficits and / or paralysis from block of motor axons and other complications from block of autonomic fibers.
This reflex, however, can became aberrant in a number of diseases leading to a non-productive dry cough where hyper- or allo-tussive states exist.
In addition, inappropriate cough reflexes can be manifested acutely and chronically following viral infection.

Method used

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  • Charged ion channel blockers and methods for use
  • Charged ion channel blockers and methods for use
  • Charged ion channel blockers and methods for use

Examples

Experimental program
Comparison scheme
Effect test

example 1

Syntheses

General Abbreviation Definitions

[0152]ACN acetonitrile[0153]aq. aqueous[0154]δ chemical shift (ppm)[0155]CDCl3 D3-chloroform[0156]DCM dichloromethane[0157]DMSO dimethyl sulfoxide[0158]ESI electrospray ionization[0159]Et2O diethyl ether[0160]EtOAc ethyl acetate[0161]h hour[0162]HPLC high pressure liquid chromatography[0163]MeOH methanol[0164]mHz megahertz[0165]MS mass spectrometry[0166]MW microwave[0167]m / z mass to charge ratio[0168]NMR nuclear magnetic resounance[0169]RT room temperature[0170]TLC thin layer chromatography[0171]UV ultraviolet light

i. Synthesis of 2-(2-((2, 6-dimethylphenyl) amino)-2-oxoethyl)-1, 4-dimethyl-1H-pyrazol-2-ium Bromide

[0172]

Synthesis of Intermediate 2-bromo-N-(2,6-dimethylphenyl)acetamide

[0173]To a suspension of 2, 6-dimethylaniline (30.5 mL, 247.56 mmol) in water (300 mL) was added bromoacetyl bromide (23.8 mL, 272.31 mmol) at 10° C. The reaction mixture was maintained at pH 9-10 with 15% Na2CO3 (aq.) solution for 1 hour as the progress of the r...

example 2

n of Nav1.7 Current

[0183]Compounds 1′A, 2′A, 3′A, 4′A and 5′A were synthesized according to the described methods and tested for the ability to inhibit voltage-gated sodium channels.

Cell Culture

[0184]NaV1.7 was expressed upon induction with tetracycline. Cells were cultured in DMEM containing 10% dialyzed Fetal Bovine Serum (VWR, Radnor, Pa.), 1% Glutamax (VWR, Radnor, Pa.), 1% Penicillin-Streptomycin (VWR, Radnor, Pa.), 100 mg / L Hygromycin (Thermo Fisher Scientific, Waltham, Mass. and 5 mg / L Blasticidin (Alfa Aesar, Haverhill, Mass.). Cells were grown and maintained at 37° C. in a humidified environment containing 10% CO2 in air. Cells were detached from the culture flask for passage and harvested using 0.05% Trypsin-EDTA (Thermo Fisher Scientific, Waltham, Mass.). To induce NaV1.7, cells were induced with tetracycline (0.1-1 μg / mL, IBI Scientific, Peosta, Iowa) the day before recording and plated onto 24-well plates. Cells were washed with DPBS (VWR, Radnor, Pa.), trypsinized and ...

example 4

Permeability

[0194]The PAMPA assay (pION, Inc., Woburn Mass.) was used to determine the ability of compounds of the invention to cross an artificial lipid membrane by passive diffusion. Test compounds were dissolved in DMSO (10 mM) and diluted 200-fold in buffer (pION Inc., pH 7.4) to provide 50 uM stock solutions. Buffer (150 μL) was added to a UV blank plate and stock solutions (150 μL) were transferred to a UV reference plate. The blank and reference spectrum were read using a spectrophotometer. Stock solutions (200 μL) were added to the donor plate of the PAMPA sandwich plate and an accept plate painted with GIT lipid (pION Inc, 5 μL) was placed on top. Buffer (200 μL) was added to the acceptor plate and the PAMPA sandwich plate was incubated for 4 hours. Aliquots (150 μL) from the acceptor plate were added to a UV plate and read as acceptor spectrum. Aliquots (150 μL) of the donor solutions were added to a UV analysis plate and read as donor spectrum. The permeability coefficien...

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PUM

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Abstract

The invention provides compounds of Formula (I), or pharmaceutically acceptable salts thereof. The compounds, compositions, methods and kits of the invention are useful for the treatment of pain, cough, itch, and neurogenic inflammation.

Description

RELATED APPLICATION[0001]This application claims the benefit of U.S. Provisional Application Ser. No. 62 / 816,441 filed Mar. 11, 2019. The entire contents of the above application are incorporated by reference herein.BACKGROUND OF THE INVENTION[0002]The invention features compounds, compositions and methods for the selective inhibition of sensory neurons (nociceptors, cough receptors and pruriceptors) and the treatment of neurogenic inflammation by targeting nociceptors with a small molecule drug, while minimizing effects on non-nociceptive neurons or other types of cells. According to the method of the invention, small, cationic drug molecules gain access to the intracellular compartment of sensory neurons via entry through large pore receptor / ion channels that are present in pain-cough-and itch-sensing neurons but to a lesser extent or not at all in other types of neurons or in other types of tissue.[0003]Local anesthetics such as lidocaine and articaine act by inhibiting voltage-d...

Claims

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Application Information

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IPC IPC(8): A61K31/415C07D231/12A61K45/06
CPCA61K31/415A61K45/06C07D231/12A61K31/4425C07D213/04C07D213/80
Inventor COLE, BRIDGET MCCARTHYELLIS, JAMES LAMOND
Owner NOCION THERAPEUTICS INC
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