| Literature DB >> 18665579 |
Andrew P Degnan1, Prasad V Chaturvedula, Charles M Conway, Deborah A Cook, Carl D Davis, Rex Denton, Xiaojun Han, Robert Macci, Neil R Mathias, Paul Moench, Sokhom S Pin, Shelly X Ren, Richard Schartman, Laura J Signor, George Thalody, Kimberly A Widmann, Cen Xu, John E Macor, Gene M Dubowchik.
Abstract
Calcitonin gene-related peptide (CGRP) has been implicated in the pathogenesis of migraine. Early chemistry leads suffered from modest potency, significant CYP3A4 inhibition, and poor aqueous solubility. Herein, we describe the optimization of these leads to give 4 (BMS-694153), a molecule with outstanding potency, a favorable predictive toxicology profile, and remarkable aqueous solubility. Compound 4 has good intranasal bioavailability in rabbits and shows dose-dependent activity in validated in vivo and ex vivo migraine models.Entities:
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Year: 2008 PMID: 18665579 DOI: 10.1021/jm800546t
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446