Related Experiment Video
Updated: Aug 23, 2026

Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
Published on: March 20, 2018
A DNA-damaging oxoaporphine alkaloid from Piper caninum
Ji Ma1, Shannon H Jones, Rebekah Marshall
1Departments of Chemistry and Biology, University of Virginia, Charlottesville, VA 22901, USA.
Abstract:
Bioassay-guided fractionation of an active organic extract of Piper caninum, using a sensitive yeast assay to monitor putative double-strand DNA-damaging activity, resulted in the isolation of the 4,5-dioxoaporphine alkaloid cepharadione A (1). Compound 1 exhibited potent inhibitory activity in a yeast cytotoxicity assay with IC(50) values of 50.2 nM toward RS321NpRAD52 grown on glucose versus 293 nM toward the same yeast strain grown on galactose.
Related Concept Videos
DNA Damage Can Stall the Cell Cycle
DNA Damage can Stall the Cell Cycle
Mutagenicity and Carcinogenicity
Spontaneous and Induced Mutations
DNA Base Pairing
Mutations
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
