Fasco M J, Dymerski P P, Wos J D, Kaminsky L S
J Med Chem. 1978 Oct;21(10):1054-9. doi: 10.1021/jm00208a009.
The metabolism of the clinically utilized, anticoagulant warfarin [4-hydroxy-3-(3-oxo-1-phenylbutyl)-2H-1-benzopyran-2-one] by rat liver microsomes has been investigated. The structure of a new warfarin metabolite [4-hydroxy-3-(3-oxo-1-phenyl-1-butenyl)-2H-1-benzopyran-2-one] (dehydrowarfarin) has been determined by mass spectral comparison with the chemically synthesized compound. The formation of dehydrowarfarin is catalyzed by cytochrome P-450 and is unusual in that the final product is effectively dehydrogenated warfarin.
已对大鼠肝微粒体对临床使用的抗凝剂华法林[4-羟基-3-(3-氧代-1-苯基丁基)-2H-1-苯并吡喃-2-酮]的代谢进行了研究。通过与化学合成化合物的质谱比较,确定了一种新的华法林代谢物4-羟基-3-(3-氧代-1-苯基-1-丁烯基)-2H-1-苯并吡喃-2-酮的结构。脱水华法林的形成由细胞色素P-450催化,其不同寻常之处在于最终产物是有效脱氢的华法林。