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Studies on enzymatic hydrolysis of aziridines. II. Stereoselective hydrolysis of N-substituted 28,38-imino-5 -cholestanes by hepatic microsomal aziridine hydrolase.

作者信息

Watabe T, Suzuki S

出版信息

Biochem Biophys Res Commun. 1972 Feb 16;46(3):1120-7. doi: 10.1016/s0006-291x(72)80090-1.

DOI:10.1016/s0006-291x(72)80090-1
PMID:5012161
Abstract
摘要

相似文献

1
Studies on enzymatic hydrolysis of aziridines. II. Stereoselective hydrolysis of N-substituted 28,38-imino-5 -cholestanes by hepatic microsomal aziridine hydrolase.
Biochem Biophys Res Commun. 1972 Feb 16;46(3):1120-7. doi: 10.1016/s0006-291x(72)80090-1.
2
Studies on enzymatic hydrolysis of aziridines. I. The conversion of 2 ,3 -imino-5 -cholestane into 2 -amino-3 -hydroxy-5 -cholestane by liver microsomes.
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3
Stereoselective hydrolysis of 2,3-epoxysteroids by hepatic microsomal epoxide hydrolase.
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Studies on enzymatic hydrolysis of aziridines. I. The conversion of 2 beta,3beta-imino-5 alpha-cholestane into 2 beta-amino-3-alpha-hydroxy-5 alpha-cholestane by liver microsomes.氮丙啶的酶促水解研究。I. 肝微粒体将2β,3β-亚氨基-5α-胆甾烷转化为2β-氨基-3α-羟基-5α-胆甾烷
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Stereoselective hydrolysis of cis- and trans-stilbene oxides by hepatic microsomal epoxide hydrolase.
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Stereoselective hydrolysis of acyclic olefin oxide to glycols by hepatic microsomal epoxide hydrolase.
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Hepatic epoxide hydrase. Structure-activity relationships for substrates and inhibitors.肝环氧水解酶。底物和抑制剂的构效关系。
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8
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