Identification of conjugation and cleavage products in the thiolytic metabolism of the anticancer drug 4′-(9-acridinylamino)methanesulfon-m-anisidide
- 1 October 1981
- journal article
- research article
- Published by Wiley in Journal of Mass Spectrometry
- Vol. 8 (10), 485-491
- https://doi.org/10.1002/bms.1200081004
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Multi-step metabolic activation of benzene. Effect of superoxide dismutase on covalent binding to microsomal macromolecules, and identification of glutathione conjugates using high pressure liquid chromatography and field desorption mass spectrometryChemico-Biological Interactions, 1980
- Biochemical, medical, and environmental applications of field-ionization and field-desorption mass spectrometryInternational Journal of Mass Spectrometry and Ion Physics, 1979
- m-AMSA and PALA: Two new agents in cancer chemotherapyCancer Chemotherapy and Pharmacology, 1979
- Field Desorption Mass Spectra of Gastrine Peptides and Glutathione DerivativesZeitschrift für Naturforschung B, 1979
- Selective Localization of 4-(9-Acridinylamino)-methanesulfon-m-anisididein B 16 MelanomaPharmacology, 1978
- Evaluation of single agents and combinations of chemotherapeutic agents in mouse colon carcinomasCancer, 1977
- Application of chemical ionization mass spectrometry and the twin-ion technique to better define a mechanism in acetylhydrazine toxicityBiochemical and Biophysical Research Communications, 1976
- Felddesorptions-MassenspektrometrieAngewandte Chemie, 1975
- Potential antitumor agents. 14. AcridylmethanesulfonanilidesJournal of Medicinal Chemistry, 1974
- The experimental antitumour properties of three congeners of the acridylmethanesulphonanilide (AMSA) seriesEuropean Journal of Cancer (1965), 1974