Uroporphyrin formation induced by chlorinated hydrocarbons (lindane, polychlorinated biphenyls, tetrachlorodibenzo-p-dioxin). Requirements for endogenous iron, protein synthesis and drug-metabolizing activity.

Biochemical and biophysical research communications ·Vol. 61 ·No. 1 ·1974-11-06 ·Pages 124-33

Sinclair PR, Granick S

Abstract

暂无摘要

MeSH Terms

Allylisopropylacetamide/pharmacology Animals Biphenyl Compounds/pharmacology Calcium/pharmacology Chelating Agents/pharmacology Chick Embryo Chromatography, Thin Layer Cycloheximide/pharmacology Edetic Acid/pharmacology Hexachlorocyclohexane/pharmacology Hydrocarbons, Chlorinated/pharmacology Iron/pharmacology Liver/drug effects,metabolism Magnesium/pharmacology Porphyrins/biosynthesis Proadifen/pharmacology Protein Biosynthesis Quinolines/pharmacology Spectrometry, Fluorescence

Chemicals

Biphenyl Compounds Chelating Agents Hydrocarbons, Chlorinated Porphyrins Quinolines Allylisopropylacetamide Hexachlorocyclohexane Cycloheximide Edetic Acid Proadifen Iron Magnesium Calcium

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Sinclair P R

Granick S

Article Info

Journal

Biochemical and biophysical research communications

Abbr.

Biochem Biophys Res Commun

ISSN

0006-291X

DOI

10.1016/0006-291x(74)90543-9

Published

1974-11-06

Pages

124-33

Language

English

Region

United States

NLM ID

0372516

Subset

External Links

PubMed source DOI: 10.1016/0006-291x(74)90543-9 View journal details

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Uroporphyrin formation induced by chlorinated hydrocarbons (lindane, polychlorinated biphenyls, tetrachlorodibenzo-p-dioxin). Requirements for endogenous iron, protein synthesis and drug-metabolizing activity.

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