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乙酰羟酸合酶抑制剂新衍生物对结核分枝杆菌和非结核分枝杆菌的体外及离体活性

In vitro and ex vivo activity of new derivatives of acetohydroxyacid synthase inhibitors against Mycobacterium tuberculosis and non-tuberculous mycobacteria.

作者信息

Sohn Hosung, Lee Kil-Soo, Ko Young-Kwan, Ryu Jae-Wook, Woo Jae-Choon, Koo Dong-Wan, Shin Sung-Jae, Ahn Se-Jin, Shin A-Rum, Song Chang-Hwa, Jo Eun-Kyeong, Park Jeong-Kyu, Kim Hwa-Jung

机构信息

Department of Microbiology, College of Medicine, Chungnam National University, 6 Munhwa-Dong, Jung-Ku, Daejeon 301-747, South Korea.

出版信息

Int J Antimicrob Agents. 2008 Jun;31(6):567-71. doi: 10.1016/j.ijantimicag.2008.01.016. Epub 2008 Mar 12.

Abstract

Sulfometuron methyl (SM) is an inhibitor of acetohydroxyacid synthase (AHAS), the first common enzyme in the branched-chain amino acid biosynthetic pathway, and shows activity against Mycobacterium tuberculosis both in vitro and in vivo. To develop AHAS inhibitor derivatives with more potent activity, 100 sulfonylurea analogues were screened for antimycobacterial activity against M. tuberculosis and non-tuberculous mycobacteria (NTM), and then evaluated for intracellular activity using mouse macrophages. Three new compounds with antimycobacterial activity comparable with that of SM were identified. These compounds exhibit significant activity against intracellular M. tuberculosis (including the drug-resistant M. tuberculosis strains), and NTM Mycobacterium abscessus and Mycobacterium kansasii, respectively.

摘要

甲基磺草酮(SM)是乙酰羟酸合酶(AHAS)的抑制剂,AHAS是支链氨基酸生物合成途径中的首个常见酶,且在体外和体内均显示出对结核分枝杆菌的活性。为了开发具有更强活性的AHAS抑制剂衍生物,筛选了100种磺酰脲类似物对结核分枝杆菌和非结核分枝杆菌(NTM)的抗分枝杆菌活性,然后使用小鼠巨噬细胞评估其细胞内活性。鉴定出三种具有与SM相当的抗分枝杆菌活性的新化合物。这些化合物分别对细胞内结核分枝杆菌(包括耐药结核分枝杆菌菌株)以及NTM脓肿分枝杆菌和堪萨斯分枝杆菌表现出显著活性。

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