| Literature DB >> 15239663 |
Marlon Cowart1, Steven P Latshaw, Pramila Bhatia, Jerome F Daanen, Jeffrey Rohde, Sherry L Nelson, Meena Patel, Teodozyi Kolasa, Masaki Nakane, Marie E Uchic, Loan N Miller, Marc A Terranova, Renjie Chang, Diana L Donnelly-Roberts, Marian T Namovic, Peter R Hollingsworth, Brenda R Martino, James J Lynch, James P Sullivan, Gin C Hsieh, Robert B Moreland, Jorge D Brioni, Andrew O Stewart.
Abstract
A new class of agents with potential utility for the treatment of erectile dysfunction has been discovered, guided by the hypothesis that selective D4 agonists are erectogenic but devoid of the side effects typically associated with dopaminergic agents. The lead agent 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole (1, ABT-724) was discovered by optimization of a series of benzimidazole arylpiperazines. This highly selective D4 agonist was found to be very potent and efficacious in vivo, eliciting penile erections in rats at a dose of 0.03 micromol/kg, with a positive response rate of 77% erectile incidence. Even at high doses, it was devoid of side effects in animal models of central nervous system behaviors, emesis, or nausea. The structure-activity relationship of the parent benzimidazole series leading to 1 is described, with the detailed in vitro and in vivo profiles described. Distinctive structural features were discovered that are associated with D4 selective agonism in this series of analogues.Entities:
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Year: 2004 PMID: 15239663 DOI: 10.1021/jm030505a
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446