Dehydrocholic acid/docusate/phenolphthalein

A racemic mixture of hydroperoxides derived non-enzymatically from linoleic acid through the action of reactive oxygen species has limited direct biological actions, such as the activation of lipoxygenases normally is rapidly reduced to

Product DescriptionEpoxide hydrolases convert the EETs into vicinal diols, with concurrent loss of much of their biological activity. It is a substrate for sheep seminal vesicle COX, producing 5,6-dihydroxy prostaglandin E1 and F1α metabolites in

Product DescriptionEpoxide hydrolases convert the EETs into vicinal diols, with concurrent loss of much of their biological activity. It is a substrate for sheep seminal vesicle COX, producing 5,6-dihydroxy prostaglandin E1 and F1α metabolites in

(DI-BR-(DI-BR-(HO-PIPERIDIN-YL-PROPOXY)-PH)-ME-ET-PHENOXY)-PIPERIDIN-YL-PROPANOL-

Product Application:(2E)-4-Methoxy-2-butenoic Acid is used in the protection of hydroxy groups in molecules forming esters such as cronate.

Product Application:(2E)-4-Methoxy-2-butenoic Acid is used in the protection of hydroxy groups in molecules forming esters such as cronate.

Product Application:(2E)-4-Methoxy-2-butenoic Acid is used in the protection of hydroxy groups in molecules forming esters such as cronate.

A bioactive metabolite of valproic acid that exhibits the same profile and potency of anticonvulsant activity in animal models as its parent compound without any observed teratogenicity and hepatotoxicity.

(E/Z)-Ginkgolic acid C17:2, isolated from Ginkgo biloba, can bind with human dihydroorotate dehydrogenase (DHODH) tightly.Form:Oil.

(E/Z)-Ginkgolic acid C17:2, isolated from Ginkgo biloba, can bind with human dihydroorotate dehydrogenase (DHODH) tightly.Form:Oil.

(L)-Dehydroascorbic acid.

(L)-Dehydroascorbic acid.