Review of Platensimycin and Platencin: Inhibitors of β-Ketoacyl-acyl Carrier Protein (ACP) Synthase III (FabH)

被引:10
|
作者
Shang, Ruofeng [1 ]
Liang, Jianping [1 ]
Yi, Yunpeng [1 ]
Liu, Yu [1 ]
Wang, Jiatu [2 ]
机构
[1] CAAS, Key Lab New Anim Drug Project Gansu Prov, Key Lab Vet Pharmaceut Dev, Minist Agr,Lanzhou Inst Husb & Pharmaceut Sci, Lanzhou 730050, Peoples R China
[2] Gansu Univ Chinese Med, Affiliated Hosp, Lanzhou 730000, Peoples R China
来源
MOLECULES | 2015年 / 20卷 / 09期
关键词
platensimycin; platencin; drug resistance; antibacterial activities; synthesis; analogues; INDUCED CASCADE CYCLIZATION; BIOLOGICAL EVALUATION; FORMAL SYNTHESIS; SELF-RESISTANCE; DISCOVERY; ANALOGS; CORE; IDENTIFICATION; BIOSYNTHESIS; DESIGN;
D O I
10.3390/molecules200916127
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Platensimycin and platencin were successively discovered from the strain Streptomyces platensis through systematic screening. These natural products have been defined as promising agents for fighting multidrug resistance in bacteria by targeting type II fatty acid synthesis with slightly different mechanisms. Bioactivity studies have shown that platensimycin and platencin offer great potential to inhibit many resistant bacteria with no cross-resistance or toxicity observed in vivo. This review summarizes the general information on platensimycin and platencin, including antibacterial and self-resistant mechanisms. Furthermore, the total synthesis pathways of platensimycin and platencin and their analogues from recent studies are presented.
引用
收藏
页码:16127 / 16141
页数:15
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