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Prostaglandins endoperoxide synthetase

Roberts, D.R. (1983) Summary Report NIOSH-EPA Interagency Agreement for the Assessment of Human Health Effects from Exposure to Di-2-(Ethylhexyl) Phthalate, Cincinnati, OH, National Institute for Occupational Safety and Health Robertson, I.G.C., Sivarajah, K., Eling, T.E. Zeiger, E. (1983) Activation of some aromatic amines to mutagenic products by prostaglandin endoperoxide synthetase. Cancer Res., 43, 476-480... [Pg.142]

Eling T, Boyd J, Reed G, et al. Xenobiotic metabolism by prostaglandin endoperoxide synthetase. Drug Metab Rev 1983 14 1023-1053. [Pg.126]

Van Der Ouderaa FJ, Buytenhek M, Nugteren DH, Van Dorp DA. Acetylation of prostaglandin endoperoxide synthetase with acetylsalicylic acid, Eur. J. Biochem. 1980 109 1-8. [Pg.306]

Van der Ouderaa, F.J. Buytenhek, M., Nugteren, D.H. and Van Dorp, D.A. (1977). Purification and characterization of prostaglandin endoperoxide synthetase from sheep vesicular glands. Biochim. Biophys. Ada, 487, 315—331... [Pg.13]

Miyamoto, T., N. Ogino, S. Yamamoto, and O. Hayaishi Purification of Prostaglandin Endoperoxide Synthetase from Bovine Vesicular Gland Microsomes. J. Biol. Chem. 251, 2629 (1976). [Pg.259]

We conclude that so far eicosapentaenoic acid has proved to be a very poor substrate for the prostaglandin endoperoxide synthetase (cyclooxygenase + peroxidase) in every species or organ tested, irrespective of whether this enzyme is connected with prostaglandin-, thromboxane- or prostacyclin-biosynthesis. [Pg.163]

Miyamoto T, Ogino N, Yamamoto S, Hayaishi O. Purification of prostaglandin endoperoxide synthetase from bovine vesicular gland microsomes. J Biol Chem 1976 251 2629-2636. [Pg.121]

Figure 3.32 Proposed mechanism for the inactivation of the cyclooxygenase component of prostaglandin endoperoxide synthetase by aspirin. Figure 3.32 Proposed mechanism for the inactivation of the cyclooxygenase component of prostaglandin endoperoxide synthetase by aspirin.
The isoxazolidine analogues of the prostaglandin endoperoxide PGH2 have been prepared from PGF2a. Both compounds are potent inhibitors of thromboxane synthetase from human platelets (Scheme 78). ... [Pg.302]

In the pharmaceutical literature some pyrazoles fused to the prostaglandin structure are cited. Thus, 9,ll-azo-PGE2 (701), a stable endoperoxide analogue that is eight times as potent as PGG2, is a compound that specifically blocks TXA2 synthetase (79MI40401). [Pg.294]

See other pages where Prostaglandins endoperoxide synthetase is mentioned: [Pg.138]    [Pg.346]    [Pg.349]    [Pg.431]    [Pg.252]    [Pg.66]    [Pg.93]    [Pg.39]    [Pg.1438]    [Pg.53]    [Pg.56]    [Pg.102]    [Pg.104]    [Pg.138]    [Pg.346]    [Pg.349]    [Pg.431]    [Pg.252]    [Pg.66]    [Pg.93]    [Pg.39]    [Pg.1438]    [Pg.53]    [Pg.56]    [Pg.102]    [Pg.104]    [Pg.126]    [Pg.167]    [Pg.1474]    [Pg.238]    [Pg.328]    [Pg.754]    [Pg.183]    [Pg.167]    [Pg.301]    [Pg.10]    [Pg.11]    [Pg.57]    [Pg.75]    [Pg.185]    [Pg.136]    [Pg.364]    [Pg.139]    [Pg.240]    [Pg.59]    [Pg.261]    [Pg.188]   
See also in sourсe #XX -- [ Pg.335 ]



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