Chain-branched 1,3-dibenzylthioureas as vanilloid receptor 1 antagonists
摘要:
A series of chain-branched 1,3-dibenzylthiourea derivatives were synthesized, and tested their antagonist activity against vanilloid receptor 1. Chain-branching led to a significant change in the mode of action and the potency. (R)-Methyl or ethyl-branched 1,3-dibenzylthiourea derivatives showed the most potent antagonist activity up to the IC50 value of 0.05 muM which is 10-fold more potent than capsazepine. (C) 2004 Elsevier Ltd. All rights reserved.
Heteroaryl Nitrile Compounds Useful as Inhibitors of Cathepsin-S
申请人:Burke Michael J.
公开号:US20130158018A1
公开(公告)日:2013-06-20
Disclosed are Cathepsin-S reversible inhibitor compounds of the formula (I) which are useful in the treatment of autoimmune and other diseases. Also disclosed are pharmaceutical compositions containing the same, and methods of making and using the same.