Conversion of des-6-methyl-2,3-oxidosqualene to 19-norlanosterol by 2,3-oxidosqualene-sterol cyclase.
作者信息
Corey E J, Krief A, Yamamoto H
出版信息
J Am Chem Soc. 1971 Mar 24;93(6):1493-4. doi: 10.1021/ja00735a034.
PMID:5548348
Abstract
摘要
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1
Conversion of des-6-methyl-2,3-oxidosqualene to 19-norlanosterol by 2,3-oxidosqualene-sterol cyclase.由2,3-氧化角鲨烯-甾醇环化酶将去-6-甲基-2,3-氧化角鲨烯转化为19-去甲羊毛甾醇。
J Am Chem Soc. 1971 Mar 24;93(6):1493-4. doi: 10.1021/ja00735a034.
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Novel A-nor sterols: synthesis and stereochemistry.新型去甲甾醇：合成与立体化学
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Artificial substrates in squalene and sterol biosynthesis.角鲨烯和甾醇生物合成中的人工底物。
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Formation of sterols by the action of 2,3-oxidosqualene-sterol cyclase on the factitious substrates 2,3:22,23-dioxidosqualene and 2,3-oxido-22,23-dihydrosqualene.通过2,3-氧化角鲨烯-甾醇环化酶对虚拟底物2,3:22,23-二氧化角鲨烯和2,3-氧化-22,23-二氢角鲨烯的作用形成甾醇。
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Some properties of the microsomal 2,3-oxidosqualene sterol cyclase.微粒体2,3-氧化角鲨烯甾醇环化酶的一些特性。
Proc Natl Acad Sci U S A. 1969 May;63(1):110-7. doi: 10.1073/pnas.63.1.110.
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The synthesis and configuration of some 32-norlanosterol derivatives.一些32-降羊毛甾醇衍生物的合成与构型
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The cyclases of triterpene and sterol biosynthesis.
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