| Literature DB >> 17391967 |
Satoshi Yoshida1, Takashi Watanabe, Yasuo Sato.
Abstract
Substituted benzoxazole derivatives which possess a nitrogen-containing heterocycle at C2 are selective partial agonists of the 5-HT(3) receptor. Alteration of substituents on the benzoxazole nucleus affords both agonist-like and antagonist-like compounds, and uniquely modifies the function of the 5-HT(3) receptor ion channel gating system. SAR and corroborative computational docking study for these partial agonists successfully explained structure and function of the 5-HT(3) receptor.Entities:
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Year: 2007 PMID: 17391967 DOI: 10.1016/j.bmc.2007.02.054
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641