Title : CYP3A4-Mediated oxygenation versus dehydrogenation of raloxifene.

Pub. Date : 2010 Jun 1

PMID : 20405834






2 Functional Relationships(s)
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1 Furthermore, it was demonstrated that 7-hydroxyraloxifene, which was previously believed to be a typical O(2)-derived metabolite of CYP3A4, is in fact produced by a highly unusual hydrolysis pathway from a putative ester, formed by the conjugation of raloxifene diquinone methide with a carboxylic acid moiety of CYP3A4, or other proteins in the reconstituted system. Esters cytochrome P450 family 3 subfamily A member 4 Homo sapiens
2 Furthermore, it was demonstrated that 7-hydroxyraloxifene, which was previously believed to be a typical O(2)-derived metabolite of CYP3A4, is in fact produced by a highly unusual hydrolysis pathway from a putative ester, formed by the conjugation of raloxifene diquinone methide with a carboxylic acid moiety of CYP3A4, or other proteins in the reconstituted system. Esters cytochrome P450 family 3 subfamily A member 4 Homo sapiens