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Bioorg Med Chem Lett ; 16(19): 5052-6, 2006 Oct 01.
Article in English | MEDLINE | ID: mdl-16889959

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.


Subject(s)
Benzodiazepines/pharmacology , Calcitonin Gene-Related Peptide Receptor Antagonists , Migraine Disorders/drug therapy , Piperidines/pharmacology , Benzodiazepines/chemical synthesis , Cyclic AMP/antagonists & inhibitors , Drug Stability , Humans , Piperidines/chemical synthesis , Protein Binding , Structure-Activity Relationship
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