Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary extracted from

  • Ohki, S.; Ogino, N.; Yamamoto, S.; Hayaishi, O.; Yamamoto, H.; Miyake, H.; Hayashi, M.
    Inhibition of prostaglandin endoperoxide synthetase by thiol analogues of prostaglandin (1977), Proc. Natl. Acad. Sci. USA, 74, 144-148.
    View publication on PubMedView publication on EuropePMC

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.14.99.1 1-Mercapto-9,11,15-trihydroxyprosta-5,13-diene inhibition of prostaglandin G1 synthesis Bos taurus
1.14.99.1 1-Mercapto-9-oxo-11,15-dihydroxyprosta-5,13-dione inhibition of prostaglandin G1 synthesis Bos taurus
1.14.99.1 2,3-Dimercaptopropanol inhibition of prostaglandin G1 synthesis Bos taurus
1.14.99.1 9,11-Dihydroxy-15S-mercaptoprosta-5,13-dienoic acid or 15R-isomer, inhibition of prostaglandin G1 synthesis Bos taurus
1.14.99.1 dihydrolipoic acid inhibition of prostaglandin G1 synthesis Bos taurus
1.14.99.1 dithiothreitol inhibition of prostaglandin G1 synthesis Bos taurus

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining

Organism

EC Number Organism UniProt Comment Textmining
1.14.99.1 Bos taurus
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.14.99.1 seminal vesicle
-
 Bos taurus
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.99.1 8,11,14-eicosatrienoic acid + O2
-
 Bos taurus prostaglandin G1 + ?
-
 ?
1.14.99.1 8,11,14-eicosatrienoic acid + O2
-
 Bos taurus prostaglandin H1 + ?
-
 ?