Suppr超能文献

2-苯基-5,6-二氢-2H-噻吩并[3,2-c]吡唑-3-醇衍生物作为细菌细胞壁生物合成的新型抑制剂

2-Phenyl-5,6-dihydro-2H-thieno[3,2-c]pyrazol-3-ol derivatives as new inhibitors of bacterial cell wall biosynthesis.

作者信息

Li Zhong, Francisco Gerardo D, Hu William, Labthavikul Pornpen, Petersen Peter J, Severin Anatoly, Singh Guy, Yang Youjun, Rasmussen Beth A, Lin Yang-I, Skotnicki Jerauld S, Mansour Tarek S

机构信息

Chemical Sciences and Infectious Diseases, Wyeth Research, Pearl River, NY 10965, USA.

出版信息

Bioorg Med Chem Lett. 2003 Aug 4;13(15):2591-4. doi: 10.1016/s0960-894x(03)00471-2.

Abstract

Twenty-five 2-phenyl-5,6-dihydro-2H-thieno[3,2-c]pyrazol-3-ol derivatives were synthesized for evaluation as new inhibitors of bacterial cell wall biosynthesis. Many of them demonstrated good inhibitory activity against Staphylococcus aureus MurB, MurC and MurD enzymes in vitro and antimicrobial activity against gram-positive bacteria including MRSA, VRE and PRSP. However, when they were tested in the presence of 4% bovine serum albumin, the MIC values increased to greater than 128 microg/mL against PRSP. None of the compounds demonstrated activity against gram-negative bacteria at MIC <32 microg/mL.

摘要

合成了25种2-苯基-5,6-二氢-2H-噻吩并[3,2-c]吡唑-3-醇衍生物,以评估其作为细菌细胞壁生物合成新抑制剂的性能。其中许多衍生物在体外对金黄色葡萄球菌MurB、MurC和MurD酶表现出良好的抑制活性,对包括耐甲氧西林金黄色葡萄球菌(MRSA)、耐万古霉素肠球菌(VRE)和耐青霉素肺炎链球菌(PRSP)在内的革兰氏阳性菌具有抗菌活性。然而,当在4%牛血清白蛋白存在的情况下进行测试时,它们对PRSP的最低抑菌浓度(MIC)值增加到大于128μg/mL。在MIC<32μg/mL时,没有一种化合物对革兰氏阴性菌表现出活性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验