Prostacyclin: evidence that intramolecular general-acid catalysis by its carboxylic acid group is responsible for the extra hydrolytic lability
- 1 July 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 108 (14) , 4192-4196
- https://doi.org/10.1021/ja00274a057
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Chemical stability of prostacyclin (PGI2) in aqueous solutionsProstaglandins, 1978
- The chemical structure of prostaglandin X (prostacyclin)Prostaglandins, 1976
- An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregationNature, 1976
- Electrostatic facilitation of general acid catalyzed .alpha.-oxonium ion formation in a lysozyme-like environment: kinetic investigationsJournal of the American Chemical Society, 1976