Design and synthesis of 2-aminothiazole based antimicrobials targeting MRSA
摘要:
Privileged structure-based libraries have been shown to provide high affinity lead compounds for a variety of important biological targets. The present study describes the synthesis and screening of a 2-aminothiazole based compound library to determine their utility as antimicrobials, focusing on MRSA. Several of the compounds in this series demonstrated improved antimicrobial activity as compared to ceftriaxone (CTX), a beta-lactam antibiotic. The most potent compound (21) had MICs in the range of 24 mu g/ml across a panel of Staphylococcus aureus strains. In addition, trifluoromethoxy substituted aminothiazoles and aminobenzothiazoles were found to be potent antimicrobials with MICs of 2-16 mu g/ml. (C) 2012 Elsevier Ltd. All rights reserved.
Compounds and Uses Thereof in Modulating Amyloid Beta
申请人:Cheng Soan
公开号:US20070260058A1
公开(公告)日:2007-11-08
Novel compounds, compositions, and kits are provided. Methods of modulating Aβ levels, and methods of treating a disease associated with aberrant Aβ levels are also provided.
COMPOUNDS AND USES THEREOF IN MODULATING AMYLOID BETA
申请人:Cheng Soan
公开号:US20100324032A1
公开(公告)日:2010-12-23
Novel compounds, compositions, and kits are provided. Methods of modulating Aβ levels, and methods of treating a disease associated with aberrant Aβ levels are also provided.