Literature DB >> 17094073

R-stereopreference analysis of lipase Novozym 435 in kinetic resolution of flurbiprofen.

Hua Yun Zhang1, Xin Wang, Chi Bun Ching.   

Abstract

Immobilized lipase from Candida antarctica (Novozym 435) was employed in the kinetic resolution of racemic flurbiprofen by enantioselective esterification with methanol. It was found that the lipase has the R-stereopreference and the reaction matches Bi Bi Ping Pong mechanism with dead-end inhibition of methanol. Furthermore, the R-stereopreference was analyzed in details from the aspects of enzymatic kinetic mechanism and reaction activation energy of both enantiomers. The R-enantiomer shows lower activation energy and higher maximum reaction rate than the S-enantiomer, which implies the R-stereopreference of the lipase and makes the kinetic resolution of flurbiprofen via enzymatic reaction feasible. (c) 2006 Wiley-Liss, Inc.

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Year:  2007        PMID: 17094073     DOI: 10.1002/chir.20347

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  1 in total

1.  Novel and Efficient Synthesis of Phenethyl Formate via Enzymatic Esterification of Formic Acid.

Authors:  Minguk Shin; Jeongbae Seo; Yesol Baek; Taek Lee; Min Jang; Chulhwan Park
Journal:  Biomolecules       Date:  2020-01-01
  1 in total

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