名称:
Design, synthesis, and SAR studies on a series of 2-pyridinylpiperazines as potent antagonists of the melanocortin-4 receptor
摘要:
A series of 2-pyridinylpiperazines derived from beta-Ala-(2,4-Cl)Phe dipeptide was synthesized for the study of their SARs and possible interactions with the MC4 receptor. Compounds such as 11k (K-i = 6.5 nM) possessed high potency. (c) 2006 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2006.04.069