Identification of 3-sulfonylindazole derivatives as potent and selective 5-HT6 antagonists
作者:Kevin G. Liu、Albert J. Robichaud、Alexander A. Greenfield、Jennifer R. Lo、Cristina Grosanu、James F. Mattes、Yanxuan Cai、Guo Ming Zhang、Jean Y. Zhang、Dianne M. Kowal、Deborah L. Smith、Li Di、Edward H. Kerns、Lee E. Schechter、Thomas A. Comery
DOI:10.1016/j.bmc.2010.10.033
日期:2011.1
develop agents for cognitive enhancement, we have been focused on the 5-HT6 receptor in order to identify potent and selective ligands for this purpose. Herein we report the identification of a novel series of 3-sulfonylindazole derivatives with acyclic amino side chains as potent and selective 5-HT6 antagonists. The synthesis and detailed SAR of this class of compounds are reported.
作为开发认知增强剂的努力的一部分,我们一直专注于5-HT 6受体,以便为此目的鉴定有效的和选择性的配体。在这里,我们报告鉴定具有有效的和选择性的5-HT 6拮抗剂的具有无环氨基侧链的一系列新的3-磺酰吲唑衍生物。报道了这类化合物的合成和详细的SAR。