Occurrence of aromatic methyl migration (NIH-shift) during oxidation of p-methylanisole by hemin-thiolester complex as a cytochrome P-450 model
- 1 October 1982
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 108 (4) , 1649-1654
- https://doi.org/10.1016/s0006-291x(82)80099-5
Abstract
No abstract availableFunding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
This publication has 13 references indexed in Scilit:
- The active site structure as thiolate-hemin-hydroxyl group coordination mode in cytochrome p-450. An approach from model investigationsInorganica Chimica Acta, 1982
- Stable hyperporphyrin spectra of hemin-dithiolate complexes using thioglycolic acid esters; a model of thiolate binding cytochrome P-450Inorganica Chimica Acta, 1981
- A model system of cytochrome P-450: Hydroxylation of aniline by iron- or hemin-thiol compound systems.CHEMICAL & PHARMACEUTICAL BULLETIN, 1979
- Aromatic methyl group migration and hydroxylation of p-toluidine by iron-thiol and hemin-thiol systems as a model of cytochrome P-450.CHEMICAL & PHARMACEUTICAL BULLETIN, 1977
- Aromatic methyl migration by iron-thiol and hemin-thiol systemsBiochemical Pharmacology, 1975
- Inert Gases: Elastic ConstantsNature, 1973
- Arene oxides and the NIH shift: The metabolism, toxicity and carcinogenicity of aromatic compoundsCellular and Molecular Life Sciences, 1972
- Metabolism of acetanilides and anisoles with rat liver microsomesBiochemical Pharmacology, 1970
- Intramolecular migration of tritium and deuterium during nonenzymic aromatic hydroxylationJournal of the American Chemical Society, 1967