Studies on enzymatic hydrolysis of aziridines—I. The conversion of 2β,3β-imino-5α-cholestane into 2β-amino-3α-hydroxy-5α-cholestane by liver microsomes-Reference-Cited by-同舟云学术

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Studies on enzymatic hydrolysis of aziridines—I. The conversion of 2β,3β-imino-5α-cholestane into 2β-amino-3α-hydroxy-5α-cholestane by liver microsomes

Published:1971-07 Issue:7 Volume:20 Page:1700-1702
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Watabe Tadashi,Kiyonaga Kazue,Hara Shoji

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference16 articles.

1. The role of arene oxide-oxepin systems in the metabolism of aromatic substrates. III. Formation of 1,2-naphthalene oxide from naphthalene by liver microsomes

2. Selective Metabolism of Cyclodiene Insecticide Enantiomers by Pig Liver Microsomal Enzymes

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1. Aziridine Formation by a Fe II /α‐Ketoglutarate Dependent Oxygenase and 2‐Aminoisobutyrate Biosynthesis in Fungi;Angewandte Chemie;2021-06-11

2. Aziridine Formation by a Fe II /α‐Ketoglutarate Dependent Oxygenase and 2‐Aminoisobutyrate Biosynthesis in Fungi;Angewandte Chemie International Edition;2021-06-11

3. Substrate Oxidation by Cytochrome P450 Enzymes;Cytochrome P450;2015

4. Variations on a (t)heme—novel mechanisms, redox partners and catalytic functions in the cytochrome P450 superfamily;Nat. Prod. Rep.;2007

5. Substrate Oxidation by Cytochrome P450 Enzymes;Cytochrome P450;2005

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