Substituted indanylacetic acids as PPAR-α–γ activators
摘要:
A series of oxazole-substituted indanylacetic acids were prepared which show a spectrum of activity as ligands for PPAR nuclear receptor subtypes. (c) 2005 Elsevier Ltd. All rights reserved.
The present invention provides compounds, pharmaceutical compositions, and methods of using such compounds or compositions for treating infection by a virus, or for affecting viral IRES activity.
本发明提供了化合物、药物组合物以及使用这些化合物或组合物治疗病毒感染或影响病毒IRES活性的方法。
Substituted indanylacetic acids as PPAR-α–γ activators
作者:Derek B. Lowe、Neil Bifulco、William H. Bullock、Thomas Claus、Philip Coish、Miao Dai、Fernando E. Dela Cruz、David Dickson、Dongping Fan、Helana Hoover-Litty、Tindy Li、Xin Ma、Gretchen Mannelly、Mary-Katherine Monahan、Ingo Muegge、Stephen O’Connor、Mareli Rodriguez、Tatiana Shelekhin、Andreas Stolle、Laurel Sweet、Ming Wang、Yamin Wang、Chengzhi Zhang、Hai-Jun Zhang、Mingbao Zhang、Kake Zhao、Qian Zhao、Jian Zhu、Lei Zhu、Manami Tsutsumi
DOI:10.1016/j.bmcl.2005.10.008
日期:2006.1
A series of oxazole-substituted indanylacetic acids were prepared which show a spectrum of activity as ligands for PPAR nuclear receptor subtypes. (c) 2005 Elsevier Ltd. All rights reserved.
ALIMOV, EH.;ISKANDAROV, S. I., DOKL. AN UZSSR,(1990) N, S. 31-34