| Literature DB >> 16889959 |
Christopher S Burgey1, Craig A Stump, Diem N Nguyen, James Z Deng, Amy G Quigley, Beth R Norton, Ian M Bell, Scott D Mosser, Christopher A Salvatore, Ruth Z Rutledge, Stefanie A Kane, Kenneth S Koblan, Joseph P Vacca, Samuel L Graham, Theresa M Williams.
Abstract
In our continuing effort to identify CGRP receptor antagonists for the acute treatment of migraine, we have undertaken a study to evaluate alternative 4-substituted piperidines to the lead dihydroquinazolinone 1. In this regard, we have identified the piperidinyl-azabenzimidazolone and phenylimidazolinone structures which, when incorporated into the benzodiazepine core, afford potent CGRP receptor antagonists (e.g., 18 and 29). These studies produced a potent analog (18) which overcomes the instability issues associated with the lead structure 1. A general pharmacophore for the 4-substituted piperidine component of these CGRP receptor antagonists is also presented.Entities:
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Year: 2006 PMID: 16889959 DOI: 10.1016/j.bmcl.2006.07.044
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823