Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Lincoln Frank H"'
Publikováno v:
Prostaglandins. 19:917-931
13,14-Dihydro-15 keto-PGE2 decomposes by first order reaction kinetics, dependent on pH, temperature and albumin concentration. Under common experimental conditions at or near neutrality in the absence of albumin decomposition is suspended with the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7520cbbd187fc37c6b3fad901f614ed
https://doi.org/10.1016/0090-6980(80)90126-4
https://doi.org/10.1016/0090-6980(80)90126-4
Publikováno v:
Journal of the American Chemical Society. 99:1222-1232
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ea3b65fd1918d64af898abb74e56bb
https://doi.org/10.1021/ja00446a039
https://doi.org/10.1021/ja00446a039
Publikováno v:
Prostaglandins. 9:5-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354562385389916543a4aa1426382eae
https://doi.org/10.1016/s0090-6980(75)80112-2
https://doi.org/10.1016/s0090-6980(75)80112-2
Publikováno v:
Prostaglandins. 20:729-733
The transformation of 6-keto-PGF1α to two prostacyclin metabolites, 2,3-dinor-6-keto-PGF1α (I) and 2,3-dinor-6,15-diketo-13,14-dihydro-PGF1α (II) by Mycobacterium rhodochrous UC-6176 is described. The finding that the bacterium oxidized 6-keto-PGF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a2bb8ae17ed54e3451a3705362bdce3
https://doi.org/10.1016/0090-6980(80)90111-2
https://doi.org/10.1016/0090-6980(80)90111-2
Autor:
Eldon G. Nidy, Udo Axen, Roy A. Johnson, Thompson John L, Lincoln Frank H, Schneider William P
Publikováno v:
Journal of the American Chemical Society. 100:7690-7705
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a580741dbc2d306362639a47ad433619
https://doi.org/10.1021/ja00492a043
https://doi.org/10.1021/ja00492a043
Publikováno v:
The Journal of Organic Chemistry. 38:951-956
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2624389f8591e39086d58031a26474b0
https://doi.org/10.1021/jo00945a024
https://doi.org/10.1021/jo00945a024
Publikováno v:
Annals of the New York Academy of Sciences. 180:76-90
Syntheses of 2 different classes of prostaglandin (PG) analogs are described that of the 3-oxa-PGs and that of the 15-methyl PGs the former of which inhibit beta-oxidative degradation and the latter of which prevent degradation by the C-15 dehydrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39ca733df466e41c9b5bf5e75d1afa30
https://doi.org/10.1111/j.1749-6632.1971.tb53186.x
https://doi.org/10.1111/j.1749-6632.1971.tb53186.x
Publikováno v:
Steroids. 11:769-786
Reaction of 16-hydroxy-17(20)-pregnen-21-oic acid methyl esters with N-(2-chloro-1,1,2-tri-fluorethyl)-diethylamine gives in high yield the corresponding 16-fluoro unsaturated esters, inversion accompanying the replacement at C-16. In a similar manne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06988ed40f5537268702739c1d8be846
https://doi.org/10.1016/s0039-128x(68)80093-5
https://doi.org/10.1016/s0039-128x(68)80093-5
Publikováno v:
Steroids. 11:755-767
Reaction of cis -17(20)-pregnen-21-oic acid methyl esters with selenium dioxide gives two 16-hydroxy steroids, a 16α-hydroxy- cis -unsaturated ester and a 16β-hydroxy- trans derivative. Reaction of the trans isomer produces mainly the 16α-hydroxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5ba2b779a899fe867ec0a5703cfdaef
https://doi.org/10.1016/s0039-128x(68)80092-3
https://doi.org/10.1016/s0039-128x(68)80092-3
Publikováno v:
Journal of the American Chemical Society. 88:3131-3133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8f47b07e7f0cde6dfc15c39dfda85be
https://doi.org/10.1021/ja00965a044
https://doi.org/10.1021/ja00965a044