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脂肪酶诺维信435在手性拆分氟比洛芬中的R-立体选择性分析

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

作者信息

Zhang Hua Yun, Wang Xin, Ching Chi Bun

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, Singapore 117576.

出版信息

Chirality. 2007 May 5;19(4):245-9. doi: 10.1002/chir.20347.

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.

摘要

利用南极假丝酵母固定化脂肪酶(诺维信435),通过与甲醇进行对映选择性酯化反应,对外消旋氟比洛芬进行动力学拆分。研究发现,该脂肪酶具有R-立体选择性,且反应符合双底物双产物乒乓机制,并存在甲醇的终产物抑制作用。此外,从酶促动力学机制和两种对映体的反应活化能方面,对R-立体选择性进行了详细分析。R-对映体比S-对映体表现出更低的活化能和更高的最大反应速率,这表明了脂肪酶的R-立体选择性,使得通过酶促反应对氟比洛芬进行动力学拆分成为可能。

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