Substitution of terminal amide with 1H-1,2,3-triazole: Identification of unexpected class of potent antibacterial agents

被引:29
作者
Bi, Fangchao [1 ]
Ji, Shengli [2 ]
Venter, Henrietta [3 ]
Liu, Jingru [1 ]
Semple, Susan J. [3 ]
Ma, Shutao [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Minist Educ, Dept Med Chem,Key Lab Chem Biol, 44 West Culture Rd, Jinan 250012, Shandong, Peoples R China
[2] ReaLi Tide Biol Technol Weihai Co Ltd, East Longhai Rd & South Yangguang Rd, Weihai 264207, Peoples R China
[3] Univ South Australia, Sansom Inst Hlth Res, Sch Pharm & Med Sci, GPO Box 2471, Adelaide, SA 5001, Australia
基金
中国国家自然科学基金;
关键词
1H-1,2,3-Triazole; Terminal amide; Mimic; Antibacterial agents; In silico prediction; BACTERIAL-CELL DIVISION; CLICK CHEMISTRY; FTSZ; DERIVATIVES; DISCOVERY; 1,2,3-TRIAZOLE; INHIBITOR; DESIGN; CHALLENGES; PC190723;
D O I
10.1016/j.bmcl.2018.02.001
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
3-Methoxybenzamide (3-MBA) derivatives have been identified as novel class of potent antibacterial agents targeting the bacterial cell division protein FtsZ. As one of isosteres for the amide group, 1,2,3-tria-zole can mimic the topological and electronic features of the amide, which has gained increasing attention in drug discovery. Based on these considerations, we prepared a series of 1H-1,2,3-triazole-containing 3-MBA analogues via isosteric replacement of the terminal amide with triazole, which had increased antibacterial activity. This study demonstrated the possibility of developing the 1H-1,2, 3-triazole group as a terminal amide-mimetic element which was capable of both keeping and modulating amide-related bioactivity. Surprisingly, a different action mode of these new 1H-1,2,3-triazole-containing analogues was observed, which could open new opportunities for the development of antibacterial agents. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:884 / 891
页数:8
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