An inorganic iron complex that inhibits wild-type and an isoniazid-resistant mutant 2-trans-enoyl-ACP (CoA) reductase from Mycobacterium tuberculosis

被引:62
作者
Oliveira, JS
Sousa, EHS
Basso, LA
Palaci, M
Dietze, R
Santos, DS
Moreira, IS
机构
[1] Univ Fed Rio Grande do Sul, Dept Mol Biol & Biotechnol, BR-91501970 Porto Alegre, RS, Brazil
[2] Univ Fed Ceara, Dept Quim Organ & Inorgan, BR-60455760 Fortaleza, Ceara, Brazil
[3] Univ Fed Espirito Santo, BR-29040091 Vitoria, ES, Spain
[4] Pontificia Univ Catolica Rio Grande do Sul, Inst Pesquisas Biomed, Fac Farm, BR-90619900 Porto Alegre, RS, Brazil
关键词
D O I
10.1039/b313592f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The in vitro kinetics of inactivation of both wild-type and I21V InhA enzymes by [Fe-II(CN)(5)(INH)](3-) indicate that this process requires no activation by KatG, and no need for the presence of NADH. This inorganic complex may represent a new class of lead compounds to the development of anti-tubercular agents aiming at inhibition of a validated target.
引用
收藏
页码:312 / 313
页数:2
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