Multi-target compound with anticoagulation and antiplatelet activity as well as preparation method and application of multi-target compound
A compound and platelet technology, applied in the field of biomedicine, can solve the problems of dose matching, affecting clinical antithrombotic effect, bleeding, etc., and achieve the effect of avoiding dose matching and reducing bleeding risk.
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[0079] One aspect of the present invention provides a preparation method of the antithrombin and platelet GPⅡb / Ⅲa receptor multi-target antagonistic compound, the method comprising the following steps: (1) adopting solid-phase synthesis method to start from the carboxyl terminal according to the polypeptide sequence Beginning to insert the corresponding protected amino acids or fragments in sequence to obtain the side chain fully protected amino acid polypeptide-Wang resin; (2) acid hydrolyzing the side chain fully protected amino acid polypeptide-Wang resin with an acid hydrolysis reagent to obtain a linear polypeptide crude product; ( 3) Cyclize the crude linear polypeptide to form a disulfide bond, and then purify it using high-pressure preparative liquid phase to obtain a polypeptide sequence.
[0080] One aspect of the present invention also provides a pharmaceutical composition, the active ingredients of which include the antithrombin and the multi-target antagonistic com...
Embodiment 1
[0092] Example 1 is used to illustrate the compound and its preparation process according to one embodiment of the present invention.
[0093] 1. Preparation of Fragment I Fmoc-Gly-Gly-Gly-Gly-OH: Weigh Fmoc-Gly-2-Cl-Trt-resin (23.5g, 16.5mmol) with a degree of substitution of 0.7mmol / g and use 2.5L 25% The PIP / DMF solution was deprotected by Fmoc for 25 minutes. After filtering, the resin was washed alternately with DMF and DCM for 3 times, each time not less than 1 minute. Fmoc-Gly-OH (14.8g, 50mmol) was added, stirred and reacted at 30°C for 4 hours, and the reaction endpoint was detected by the ninhydrin method. After the reaction was completed, the resin was filtered and washed alternately with DMF and DCM three times respectively.
[0094] Repeat the above steps 2 times to connect another 2 Gly to finally obtain Fmoc-Gly-Gly-Gly-Gly-2-Cl-Trt-resin. The obtained resin was dissolved in 5 L of 30% hexafluoroisopropanol / DCM solution, stirred and reacted for 2 hours, the fil...
Embodiment 2
[0102] The polypeptide compound 2 was prepared according to the same method as in Example 1, except that the L' fragment was Glu Ala AlaAla Lys to obtain polypeptide 2, and the product quality was 1.2 g. The mass spectrometry detection results of polypeptide 2 are as follows: figure 2 shown.
[0103] The structural formula of polypeptide 2 is as follows (peptide sequence shown in SEQ ID No.5): D-Phe Pro Arg Pro GlyGly Gly Gly Asn Gly Asp Phe Glu Glu Ile Pro Glu Glu Tyr Leu Glu Ala Ala AlaLys Cys Har Gly Asp Trp Pro Cys
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