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
相关论文
共 50 条
  • [41] Microbial/enzymatic synthesis of chiral intermediates for pharmaceuticals
    Patel, RN
    ENZYME AND MICROBIAL TECHNOLOGY, 2002, 31 (06) : 804 - 826
  • [42] CHIRAL SYNTHESIS OF THE KEY INTERMEDIATES OF (+)-THIENAMYCIN AND (-)-THIENAMYCIN
    KAMETANI, T
    NAGAHARA, T
    HONDA, T
    JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (13): : 2327 - 2331
  • [43] Captopril and its synthesis from chiral intermediates
    Chirumamilla, RR
    Marchant, R
    Nigam, P
    JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2001, 76 (02) : 123 - 127
  • [44] Pharmaceutical intermediates
    Schmitt, Bill
    Morrison, Scott
    Mullin, Rick
    Chemical Week, 2002, 164 (08) : 27 - 38
  • [45] Pharmaceutical intermediates
    Anon
    Chemical and Engineering News, 2001, 79 (44):
  • [46] PROCESS DEVELOPMENT WITH BIFUNCTIONAL CHIRAL EPOXIDES TO ACCESS SINGLE ENANTIOMERS OF PHARMACEUTICAL INTERMEDIATES
    Ikunaka, Masaya
    Sugai, Takeshi
    JOURNAL OF OIL PALM RESEARCH, 2008, : 143 - 158
  • [47] Functional plasticity of medium-chain dehydrogenases/reductases
    Riveros-Rosas, H
    Julián-Sánchez, A
    ENZYMOLOGY AND MOLECULAR BIOLOGY OF CARBONYL METABOLISM 12, 2006, 12 : 419 - 433
  • [48] Comparative functional analysis of human medium-chain dehydrogenases, short-chain dehydrogenases/reductases and aldo-keto reductases with retinoids
    Gallego, Oriol
    Belyaeva, Olga V.
    Porte, Sergio
    Ruiz, F. Xavier
    Stetsenko, Anton V.
    Shabrova, Elena V.
    Kostereva, Natalia V.
    Farres, Jaume
    Pares, Xavier
    Kedishvili, Natalia Y.
    BIOCHEMICAL JOURNAL, 2006, 399 : 101 - 109
  • [49] Expanding the Application of Alcohol Dehydrogenases in Pharmaceutical Chemistry: A Focus on Piperidone Synthesis
    Li, Fulong
    Wei, Yuwen
    Du, Yan
    Liang, Youxiang
    Zheng, Yukun
    Yuan, Shuting
    Yu, Huimin
    CHEMCATCHEM, 2024, 16 (11)
  • [50] Systematic Evaluation of Imine-Reducing Enzymes: Common Principles in Imine Reductases, β-Hydroxy Acid Dehydrogenases, and Short-Chain Dehydrogenases/Reductases
    Stockinger, Peter
    Roth, Sebastian
    Mueller, Michael
    Pleiss, Juergen
    CHEMBIOCHEM, 2020, 21 (18) : 2689 - 2695