Structure–activity relationships of 6-(aminomethylphenoxy)-benzoxaborole derivatives as anti-inflammatory agent
摘要:
A series of novel 6-(aminomethylphenoxy)benzoxaborole analogs was synthesized for the investigation of the structure-activity relationship of the inhibition of TNF-alpha, IL-1beta, and IL-6, from lipopolysaccharide stimulated peripheral blood mononuclear cells. Compounds 9d and 9e showed potent activity against all three cytokines with IC50 values between 33 and 83 nM. Chloro substituted analog 9e (AN3485) is considered to be a promising lead for novel anti-inflammatory agent with a favorable pharmacokinetic profile. (C) 2013 Elsevier Ltd. All rights reserved.
This invention relates to, among other items, 6-substituted benzoxaborole compounds and their use for treating bacterial infections.
这项发明涉及6-取代苯硼酯化合物等物品,以及它们用于治疗细菌感染的用途。
Structure–activity relationships of 6-(aminomethylphenoxy)-benzoxaborole derivatives as anti-inflammatory agent
作者:Tsutomu Akama、Charlotte Virtucio、Chen Dong、Richard Kimura、Yong-Kang Zhang、James A. Nieman、Rashmi Sharma、Xiaosong Lu、Marcelo Sales、Rajeshwar Singh、Anne Wu、Xiao-Qing Fan、Liang Liu、Jacob J. Plattner、Kurt Jarnagin、Yvonne R. Freund
DOI:10.1016/j.bmcl.2013.01.072
日期:2013.3
A series of novel 6-(aminomethylphenoxy)benzoxaborole analogs was synthesized for the investigation of the structure-activity relationship of the inhibition of TNF-alpha, IL-1beta, and IL-6, from lipopolysaccharide stimulated peripheral blood mononuclear cells. Compounds 9d and 9e showed potent activity against all three cytokines with IC50 values between 33 and 83 nM. Chloro substituted analog 9e (AN3485) is considered to be a promising lead for novel anti-inflammatory agent with a favorable pharmacokinetic profile. (C) 2013 Elsevier Ltd. All rights reserved.