Related Experiment Video
Updated: Aug 14, 2026

A General Method for Detecting Nitrosamide Formation in the In Vitro Metabolism of Nitrosamines by Cytochrome P450s
Published on: September 25, 2017
Sulfonation in chemical carcinogenesis--history and present status
1McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706.
Abstract:
Many laboratories have characterized the electrophilic metabolites of chemical carcinogens and their covalently bound adducts with genomic DNA in vivo. Recent studies from our laboratory have shown that enzymatic sulfonation of members of several classes of proximate carcinogens containing C- or N-hydroxy groups converts them to electrophilic, mutagenic, and carcinogenic sulfuric acid ester metabolites in mouse liver. These compounds form the subject of this report.
More Related Videos
09:33Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
Published on: March 20, 2018
14:20High Throughput SiRNA Screening for Chloropicrin and Hydrogen Fluoride-Induced Cornea Epithelial Cell Injury
Published on: June 16, 2018
Related Concept Videos
Preparation and Reactions of Sulfides
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Mutagenicity and Carcinogenicity
Phase II Reactions: Sulfation and Conjugation with α-Amino Acids
Phase II Reactions: Miscellaneous Conjugation Reactions
A key example involves the conjugation of cyanide ions, which impair cellular respiration and alter hemoglobin into non-oxygen-carrying cyanmethemoglobin. To neutralize this threat, a sulfur atom from thiosulphate is transferred to the cyanide ion, catalyzed by the enzyme rhodanese, resulting in an inactive compound called thiocyanate. The production of...
Sulfur Assimilation