Synthesis of coenzyme A ester of retinoic acid: intermediate in vitamin A metabolism.
AUTOR(ES)
Kutner, A
RESUMO
Coenzyme A esters of all-trans- and 13-cis-retinoic acid were synthesized for use in studying vitamin A metabolism. The esters were obtained by two different synthetic methods starting from retinoic acids, which were converted to activated succinimidyl esters or anhydrides. These in turn were coupled with coenzyme A to form their respective thioesters. The retinoyl coenzyme A esters were purified by reverse-phase high performance liquid chromatography.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=386593Documentos Relacionados
- In Vitro Synthesis of Poliovirus Ribonucleic Acid: Role of the Replicative Intermediate
- Targeted disruption of retinoic acid receptor alpha (RAR alpha) and RAR gamma results in receptor-specific alterations in retinoic acid-mediated differentiation and retinoic acid metabolism.
- Candida lipolytica mutants defective in an acyl-coenzyme A synthetase: isolation and fatty acid metabolism.
- Alginic acid synthesis in Pseudomonas aeruginosa mutants defective in carbohydrate metabolism.
- Multiple sclerosis and vitamin B12 metabolism.