Discovery and Syntheses of "Superbug Challengers"-Platensimycin and Platencin

被引:61
作者
Palanichamy, Kalanidhi [1 ]
Kaliappan, Krishna P. [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India
关键词
antibiotics; bacterial infection; fatty acids; platencin; platensimycin; DIELS-ALDER REACTIONS; FATTY-ACID SYNTHESIS; ASYMMETRIC ALLYLIC ALKYLATION; FORMAL TOTAL-SYNTHESIS; SILYL ENOL ETHERS; PALLADIUM-CATALYZED HYDROGENOLYSIS; ENANTIOSELECTIVE TOTAL-SYNTHESIS; RADICAL-TYPE CYCLIZATION; ENZYME-BOUND STRUCTURE; SYNTHASE-III FABH;
D O I
10.1002/asia.200900423
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bacteria have developed resistance to almost all existing antibiotics known today and this has been a major issue over the last few decades. The search for a new class of antibiotics with a new mode of action to fight these multiply-drug-resistant strains, or "superbugs", allowed a team of scientists at Merck to discover two novel antibiotics, platensimycin and platencin using advanced screening strategies, as inhibitors of bacterial fatty acid biosynthesis, which is essential for the survival of bacteria. Though both these antibiotics are structurally related. they work by slightly different mechanisms and target different enzymes conserved in the bacterial fatty acid biosynthesis. This Focus Review summarizes the synthetic and biological aspects of these natural products and their analogues and congeners.
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收藏
页码:668 / 703
页数:36
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