Dehydrogenases/Reductases for the Synthesis of Chiral Pharmaceutical Intermediates

被引:31
|
作者
Huang, Yan [1 ]
Liu, Nan [1 ]
Wu, Xuri [1 ]
Chen, Yijun [1 ]
机构
[1] China Pharmaceut Univ, Biol Chem Lab, Nanjing 210009, Jiangsu, Peoples R China
关键词
Biocatalysis; Dehydrogenases; Reductases; Chiral intermediates; Stereoselectivity; Cofactor regeneration; ETHYL 4-CHLORO ACETOACETATE; SITE-DIRECTED MUTAGENESIS; ENANTIOSELECTIVE MICROBIAL REDUCTION; BIOCATALYTIC KETONE REDUCTION; ADRENERGIC-RECEPTOR AGONISTS; CONVERTING ENZYME ACE; ALCOHOL-DEHYDROGENASE; ASYMMETRIC REDUCTION; GENE CLONING; ACTIVE-SITE;
D O I
10.2174/138527210791616795
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The increasing trend of chiral drugs in the pharmaceutical industry has promoted greatly on the development of numerous biocatalytic routes in combination with chemical methods. Because the resulting chiral alcohols are particularly valuable intermediates and precursors for the synthesis of chiral drugs, dehydrogenases and reductases have been extensively used in the synthesis of chiral compounds from ketone substrates with high regio- and stereo-selectivities. In this review, biocatalytic processes carried out by dehydrogenases and reductases are described for the synthesis of chiral intermediates for a wide variety of pharmaceuticals, including antidepressants, anti-anxieties, anti-asthmatics, anti-hypertensives, cholesterol-lowering agents, NK1 antagonists, ACE inhibitors and beta-Lactamase inhibitors.
引用
收藏
页码:1447 / 1460
页数:14
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