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16 -methyl-prostaglandin

Williams, J.H., Jr. R.D. Fairshter, T.R. Ulich, S. Crosby, M. Chen, L. Rosario, and N.D. Vaziri. 1988. Adverse effects of (155)-15-methyl-prostaglandin Ej in normal and paraquat-exposed rats. Toxicol. Appl. Pharmacol. 92 330-334. [Pg.1192]

Hemal AK, Vaidyanathan S, Sankaranarayanan A, Ayyagari S, Sharma PL. Control of massive vesical hemorrhage due to radiation cystitis with intravesical instillation of 15 (s) 15-methyl prostaglandin F2-alpha. Int J Clin Pharmacol Ther Toxicol 1988 26(10) 477-8. [Pg.110]

Rodriguez de la Torre MR, Gallego Alonso JI, Gil Fernandez M. Edema pulmonar en una cesarea relacionado con la administracion de 15-metil prostaglandina F2 alpha. [Pulmonary edema related to administration of 15-methyl-prostaglandin F2 alpha during a cesarean section.] Rev Esp Anestesiol Reanim 2004 51(2) 104-7. [Pg.117]

Biswas A, Roy S. A comparative study of the efficacy and safety of synthetic prostaglandin E2 derivative and 15-methyl prostaglandin F2 alpha in the termination of midtrimester pregnancy. J Indian Med Assoc 1996 94(8) 292-3. [Pg.117]

Duenhoelter, J. Ramos, R. Milewich, L. MacKonald, P. Interruption of early pregnancy with a silastic device containing (15S)-15-methyl prostaglandin F2 alpha Methyl Ester efficacy and Mode of Action. Contraception 1978,17, 51. [Pg.1359]

Spilman, C. Roseman, T. Luteolytic and abortifacient effects in rhesus monkeys of silicone vaginal rings containing 15(S) 15-methyl-prostaglandin F2 alpha methyl ester. Contraception 1975, 11, 409-18. [Pg.1359]

The same compound has also been used to prepare 11-deoxy-lla-hydroxy-methyl prostaglandin Es 239). [Pg.140]

An important pathway for in vivo deactivation of prostaglandin A2 is the rapid conversion in mammalian blood via prostaglandin C2 to the more stable and biologically inactive prostaglandin 82-12-Methyl PGA2 and 8-methyl PGC2 were synthesized because they cannot be deactivated by this pathway. [Pg.291]

Absorption spectroscopy provides an opportunity to follow concentrations of individual species with time by observing the system at more than one wavelength. An example is the dehydration of prostaglandin E methyl ester, in which the essential chemistry is shown as follows ... [Pg.72]

See other pages where 16 -methyl-prostaglandin is mentioned: [Pg.275]    [Pg.116]    [Pg.433]    [Pg.481]    [Pg.647]    [Pg.795]    [Pg.134]    [Pg.205]    [Pg.413]    [Pg.328]    [Pg.284]    [Pg.1165]    [Pg.275]    [Pg.1165]    [Pg.116]    [Pg.433]    [Pg.481]    [Pg.647]    [Pg.795]    [Pg.275]    [Pg.315]    [Pg.396]    [Pg.134]    [Pg.205]    [Pg.1028]    [Pg.578]    [Pg.413]    [Pg.413]    [Pg.328]    [Pg.380]    [Pg.255]    [Pg.165]    [Pg.444]    [Pg.166]   
See also in sourсe #XX -- [ Pg.320 ]



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