| Literature DB >> 15837306 |
Miyuki Tatsuta1, Mikayo Kataoka, Kayo Yasoshima, Sachiko Sakakibara, Yuka Shogase, Makoto Shimazaki, Takeshi Yura, Yingfu Li, Noriyuki Yamamoto, Jang Gupta, Klaus Urbahns.
Abstract
1-(1H-Benzimidazol-5-yl)-3-tert-butylurea derivatives have been identified as a novel class of non-peptide luteinizing hormone-releasing hormone (LHRH) antagonists. Herein, we disclose the synthesis and structure-activity relationships (SAR) of this class resulting in the identification of compound 12c, with dual functional activity on human and rat receptors (rat LHRH: IC50=120 nM; human LHRH: IC50=18 nM). These SAR studies suggest that 1-(1H-benzimidazol-5-yl)-3-tert-butylurea is a new pharmacophore for small molecule LHRH antagonists.Entities:
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Year: 2005 PMID: 15837306 DOI: 10.1016/j.bmcl.2005.03.030
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823