Talk:Coronaric acid
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assorted problems
editOccurrence - such as (Helianthus annus) - delete ( & )
metabolize linoleic acid to (+)12?S,13?R-epoxy-9?(Z)-octadecaenoic acid and (-)12?R,13?S-epoxy-9?(Z)-octadecaenoic acid, i.e. the (+) and (-) epoxy optical isomers of coronaric acid
This? same CYP epoxygenases
carbon 9?,10? rather than 12?,13? double bond
9?S,10?R-epoxy-12?(Z)-octadecaenoic and 9?R,10?S-epoxy-12?(Z)-octadecaenoic acids. This (+) and (-) optical mixture is often termed vernolic acid or? when studied in plants and leukotoxin when studied in mammals (and optical should either be deleted or changed to optical isomer)
Coronoric? acid is found in urine
as a result of the spontaneous process of autooxidation.[7] This autoxidation - inconsistent autooxidation vs. autoxidation
Toxicities - to that of other structurally unrelated leukotoxins viz., - delete ,
and when injected into rodents produce? (add s)
counterparts, 9S,10R- and 9R,10S-dihydroxy-12(Z)-octadecaenoic acids by soluable - either delete , after counterparts or add , after acids
acting primarily if not exclusively through its dihydroxy counterparts, is responsible for or contribute? (add s)
Vernolic acid (i.e. leukotoxin) shares a similar metabolic fate in being converted by soluble epoxide hydrolase to its dihydroxy counterparts and? toxic actions of these hydroxide counterparts
Other activities - with the epoxides of arachidonic acid, i.e. the epoxyeicosatreienoates?
108.18.223.247 (talk) 07:57, 11 November 2020 (UTC)