Discovery and syntheses of "superbug challengers"-platensimycin and platencin
DSpace at IIT Bombay
View Archive InfoField | Value | |
Title |
Discovery and syntheses of "superbug challengers"-platensimycin and platencin
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Creator |
PALANICHAMY, K
KALIAPPAN, KP |
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Subject |
antibiotics
bacterial infection fatty acids platencin platensimycin diels-alder reactions fatty-acid synthesis silyl enol ethers asymmetric allylic alkylation formal total-synthesis alpha,beta-unsaturated carbonyl-compounds palladium-catalyzed hydrogenolysis enantioselective total-synthesis polyvalent iodine compounds radical-type cyclization |
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Description |
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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Publisher |
WILEY-V C H VERLAG GMBH
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Date |
2011-10-12T11:40:43Z
2011-12-15T09:16:06Z 2011-10-12T11:40:43Z 2011-12-15T09:16:06Z 2010 |
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Type |
Review
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Identifier |
CHEMISTRY-AN ASIAN JOURNAL,5(4)668-703
1861-4728 http://dx.doi.org/10.1002/asia.200900423 http://dspace.library.iitb.ac.in/xmlui/handle/10054/13761 http://hdl.handle.net/100/2995 |
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Language |
en
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