๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Effect of 13-hydroperoxy-9,11-octadecadienoic acid (13-hpode) on arachidonic acid metabolism in rabbit platelets

โœ Scribed by Fujimoto Yohko; Sumiya Toshiki; Tsunomori Masahide; Nlshida Hlroko; Sakuma Satoru; Fujita Tadashi


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
482 KB
Volume
26
Category
Article
ISSN
0020-711X

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Vanadium-catalyzed transformation of 13(
โœ Mats Hamberg ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 643 KB

Treatment of methyl 13(S)-hydroperoxy-9(Z),ll(E)-octadecadienoate with vanadium oxyacetylacetonate led to the formation of two diastereomeric ~,#-epoxy alcohols, i.e. methyl ll(R),12(R).epoxy-13(S)-hydroxy-9(Z)-octadecenoate and methyl ll(S),12(S)-epoxy-13(S)hydroxy-9(Z)-octadecenoate. The epoxy alc

Photolysis of unsaturated fatty acid hyd
โœ P. Schieberle; Yezid Trebert; Joachim Firl; Werner Grosch ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 599 KB

In the presence of oxygen, UV-irradiation of a solution of methyl 13(S)-hydroperoxy-9(Z), 1 l(E)-octadecadienoate (13-HPOD) in cyclohexane leads to a broad pattern of reaction products of which a trihydroxyene, seven epoxyhydroxides, four hydroxydienes, four epoxyhydroperoxides, six oxodienes and an

Photolysis of unsaturated fatty acid hyd
โœ Peter Schieberle; Yezid Trebert; Joachim Firl; Werner Grosch ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 764 KB

A solution of methyl 13(S)-hydroperoxy-9(Z),ll(E)-octadecadienoate (13-HPOD)in methanol was irradiated under anaerobic conditions at 15ยฐC with light at wavelengths greater than 230 nm. After 2 h the 13-HPOD was completely degraded and four major products were formed. Three of them were identified as

Photolysis of unsaturated fatty acid hyd
โœ Peter Schieberle; Yezid Trebert; Joachim Firl; Werner Grosch ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 799 KB

in the presence of oxygen, UV-irradiation of a solution of methyl 13(S)-hydroperoxy-9(Z),l I(E)octadecadienoate (13-HPOD) in methanol yields stereoisomers of methyl 9,13-dihydroxy-10methoxy-1 l(E)-octadecenoate and methyl 9,13-dihydroxy-12-methoxy-10(E)-octadecenoate as major products. The reaction