降钙素基因相关肽
生物利用度
化学
偏头痛
药理学
降钙素
体内
敌手
受体
口服
肽
内科学
生物化学
神经肽
医学
生物
生物技术
作者
Stephen E. Mercer,Prasad V. Chaturvedula,Charles M. Conway,Deborah A. Cook,Carl D. Davis,Sokhom S. Pin,Robert Macci,Richard Schartman,Laura J. Signor,Kimberly A. Widmann,Valerie Whiterock,Ping Chen,Cen Xu,John J. Herbst,Walter A. Kostich,George Thalody,John E. Macor,Gene M. Dubowchik
标识
DOI:10.1016/j.bmcl.2020.127624
摘要
Calcitonin gene-related peptide (CGRP) receptor antagonists have been shown clinically to be effective treatments for migraine. Zavegepant (BHV-3500, BMS-742413) is a high affinity antagonist of the CGRP receptor (hCGRP Ki = 0.023 nM) that has demonstrated efficacy in the acute treatment of migraine with intranasal delivery in a Phase 2/3 trial, despite showing low oral bioavailability in rats (FPO = 1.7%). Using zavegepant as a template, we sought to improve oral bioavailability through a series of azepinones which were designed in an attempt to reduce the number of rotatable bonds. These efforts led to the discovery of compound 21 which was able to mostly maintain high affinity binding (hCGRP Ki = 0.100 nM) and in vivo efficacy in the marmoset facial blood flow assay, while greatly improving oral bioavailability (rat FPO = 17%).
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