Discovery of 2-iminobenzimidazoles as a new class of trypanothione reductase inhibitor by high-throughput screening.

Discovery of 2-iminobenzimidazoles as a new class of trypanothione reductase inhibitor by high-throughput screening.
复制标题

DOI:
10.1016/j.bmcl.2006.11.090
复制
发表时间:
2007-03-01
影响因子:
2.7
通讯作者:
Street IP
Street IP
中科院分区:
医学4区
文献类型:
--
作者:
Holloway GA;Baell JB;Fairlamb AH;Novello PM;Parisot JP;Richardson J;Watson KG;Street IP

文献摘要

参考文献

被引文献

相似文献

一项对100,000种铅样化合物的库进行的高通量筛选活动将2-亚氨基苯并咪唑鉴定为一类新的锥虫硫酮还原酶抑制剂。这些2-亚氨基苯并咪唑显示出对布氏罗得西亚锥虫的有效杀锥虫活性,不抑制密切相关的人谷胱甘肽还原酶,并且对哺乳动物细胞具有低细胞毒性。
A high-throughput screening campaign of a library of 100,000 lead-like compounds identified 2-iminobenzimidazoles as a novel class of trypanothione reductase inhibitors. These 2-iminobenzimidazoles display potent trypanocidal activity against Trypanosoma brucei rhodesiense, do not inhibit closely related human glutathione reductase and have low cytotoxicity against mammalian cells.
DOI: 10.1016/j.bmcl.2006.03.048
发表时间: 2006-06-15
影响因子: 2.7
作者:
Bi, Xiangdong;Lopez, Christina;Woster, Patrick M.
通讯作者: Woster, Patrick M.
DOI: 10.1046/j.1365-2958.1998.00968.x
发表时间: 1998-07-01
影响因子: 3.6
作者:
Tovar, J;Wilkinson, S;Fairlamb, AH
通讯作者: Fairlamb, AH
DOI: 10.1021/ci010366a
发表时间: 2001-09-01
期刊: JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES
影响因子: --
作者:
Oprea, TI;Davis, AM;Leeson, PD
通讯作者: Leeson, PD
DOI: 10.1042/bj20021298
发表时间: 2003-02-01
影响因子: 4.1
作者:
Hamilton, CJ;Saravanamuthu, A;Fairlamb, AH
通讯作者: Fairlamb, AH