Autocatalytic alkylation of the cytochrome P-450 prosthetic haem group by 1-aminobenzotriazole. Isolation of an NN-bridged benzyne-protoporphyrin IX adduct

Destruction of hepatic cytochrome P-450 during catalytic processing of 1-amino-benzotriazole is accompanied by an equal loss of microsomal haem but not by loss of cytochrome b5, or stimulation of lipid peroxidation. An abnormal porphyrin, tentatively identified as an NN-bridged benzyne-protoporphyri...

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Veröffentlicht in:Biochemical journal 1981-06, Vol.195 (3), p.761-764
Hauptverfasser: Ortiz de Montellano, P R, Mathews, J M
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container_title Biochemical journal
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creator Ortiz de Montellano, P R
Mathews, J M
description Destruction of hepatic cytochrome P-450 during catalytic processing of 1-amino-benzotriazole is accompanied by an equal loss of microsomal haem but not by loss of cytochrome b5, or stimulation of lipid peroxidation. An abnormal porphyrin, tentatively identified as an NN-bridged benzyne-protoporphyrin IX adduct, appears to be formed by the addition of catalytically generated benzyne to prosthetic haem.
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection
subjects Alkylation
Animals
Cytochrome P-450 Enzyme Inhibitors
Cytochromes - metabolism
Cytochromes b5
Heme - metabolism
In Vitro Techniques
Macromolecular Substances
Male
Microsomes, Liver - drug effects
Microsomes, Liver - enzymology
Protoporphyrins - isolation & purification
Rats
Rats, Inbred Strains
Spectrophotometry
Triazoles - pharmacology
title Autocatalytic alkylation of the cytochrome P-450 prosthetic haem group by 1-aminobenzotriazole. Isolation of an NN-bridged benzyne-protoporphyrin IX adduct
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