Discovery of a new binding mode for a series of liver X receptor agonists
摘要:
Structural modification of a series of dual LXR alpha/beta agonists led to the identification of a new class of LXR beta partial agonists. An X-ray co-crystal structure shows that a representative member of this series, pyrrole 5, binds to LXR beta with a reversed orientation compared to 1. (C) 2012 Elsevier Ltd. All rights reserved.
Arylsulfonamidobenzyl alcohols, amines and sulfonamides are provided which are useful in treating lipid disorders, metabolic diseases and cell-proliferative diseases.
Heterocyclic arylsulfonamidobenzylic compounds are provided which are useful in treating lipid disorders, metabolic disorders and cell-proliferative diseases.