4-Substituted anilides as selective melatonin MT 2 receptor agonists
摘要:
A series of 4-substituted anilides with human melatonergic affinity is reported. Butyramides 26, 39, 42, 52, 57, and 58 all demonstrated subnanomolar MT2 binding affinity and MT2 selectivity of at least 70-fold over the MT1 receptor. Compound 26 demonstrated full agonism at the MT2 receptor. (C) 2003 Elsevier Ltd. All rights reserved.
4-Substituted anilides as selective melatonin MT 2 receptor agonists
作者:James R. Epperson、Jeffrey A. Deskus、Anthony J. Gentile、Lawrence G. Iben、Elaine Ryan、Nathan S. Sarbin
DOI:10.1016/j.bmcl.2003.11.030
日期:2004.2
A series of 4-substituted anilides with human melatonergic affinity is reported. Butyramides 26, 39, 42, 52, 57, and 58 all demonstrated subnanomolar MT2 binding affinity and MT2 selectivity of at least 70-fold over the MT1 receptor. Compound 26 demonstrated full agonism at the MT2 receptor. (C) 2003 Elsevier Ltd. All rights reserved.