A high-performance liquid chromatographic method for the enantiomeric analysis of the enzymatically synthesized coenzyme A ester of 2-tetradecylglycidic acid-Reference-Cited by-同舟云学术

A high-performance liquid chromatographic method for the enantiomeric analysis of the enzymatically synthesized coenzyme A ester of 2-tetradecylglycidic acid

Published:1987-02 Issue:2 Volume:160 Page:316-322
ISSN:0003-2697
Container-title:Analytical Biochemistry
language:en
Short-container-title:Analytical Biochemistry

Author:

Weaner Larry E.,Hoerr David C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference23 articles.

1. Mechanism of Hyperglycemia and Response to Treatment with an Inhibitor of Fatty Acid Oxidation in a Patient with Insulin Resistance due to Antiinsulin Receptor Antibodies*

2. Identification of 2-tetradecylglycidyl coenzyme A as the active form of methyl 2-tetradecylglycidate (methyl palmoxirate) and its characterization as an irreversible, active site-directed inhibitor of carnitine palmitoyltransferase A in isolated rat liver mitochondria.

3. Inhibition of hepatic lipogenesis by 2-tetradecylglycidic acid

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1. Evaluation of Free Fatty Acid Metabolism in Vivo;Annals of the New York Academy of Sciences;2006-01-24

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3. Lipase-Catalyzed Enantioselective Synthesis of Methyl (R)- and (S)-2-Tetradecyloxiranecarboxylate through Sequential Kinetic Resolution;The Journal of Organic Chemistry;1997-05-01

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