Chiral inversion of 2-arylpropionic acid non-steroidal anti-inflammatory drugs—II Racemization and hydrolysis of (R)- and (S)-ibuprofen-CoA thioesters-Reference-Cited by-同舟云学术

Chiral inversion of 2-arylpropionic acid non-steroidal anti-inflammatory drugs—II Racemization and hydrolysis of (R)- and (S)-ibuprofen-CoA thioesters

Published:1991-10 Issue:10 Volume:42 Page:1905-1911
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Knihinicki Romualda D.,Day Richard O.,Williams Kenneth M.

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference16 articles.

1. The metabolic chiral inversion of 2-arylpropionic acids. A novel route with pharmacological consequences;Hutt;J Pharm Pharmacol,1983

2. Optical isomerization mechanism of R(−)- hydratropic acid derivatives;Nakamura;Pharmacobiodynamics,1981

3. Enantiospecific formation of fenoprofen coenzyme A thioesters in vitro;Knights;Biochem Pharmacol,1988

4. Chiral inversion of 2- arylpropionic acid non-steroidal anti-inflammatory drugs 1. In vitro studies of ibuprofen and flurbiprofen;Knihinicki;Biochem Pharmacol,1989

5. Stereoselective arylpropionyl-CoA thioester formation in vitro;Knadler;Chirality,1990

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