Molecular cytotoxic mechanisms of anticancer hydroxychalcones
- 30 June 2004
- journal article
- Published by Elsevier BV in Chemico-Biological Interactions
- Vol. 148 (1-2), 57-67
- https://doi.org/10.1016/j.cbi.2004.04.004
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Apoptosis Induced by Isoliquiritigenin in Human Gastric Cancer MGC-803 CellsPlanta Medica, 2001
- Curcumin–glutathione interactions and the role of human glutathione S-transferase P1-1Chemico-Biological Interactions, 2000
- Dietary ortho phenols that induce glutathione S-transferase and increase the resistance of cells to hydrogen peroxide are potential cancer chemopreventives that act by two mechanisms: the alleviation of oxidative stress and the detoxification of mutagenic xenobioticsCancer Letters, 2000
- Synthesis and Anti-inflammatory Effect of ChalconesJournal of Pharmacy and Pharmacology, 2000
- On the toxicity of phenols to fast growing cells. A QSAR model for a radical-based toxicityJournal of the Chemical Society, Perkin Transactions 2, 1999
- Anticancer and antioxidant activity of synthetic chalcones and related compoundsCancer Letters, 1995
- Synthesis and Pharmacological Evaluation of 2'-Hydroxychalcones and Flavones as Inhibitors of Inflammatory Mediators GenerationJournal of Medicinal Chemistry, 1995
- Inhibitory effects of 3′‐methyl‐3‐hydroxy‐chalcone on proliferation of human malignant tumor cells and on skin carcinogenesisInternational Journal of Cancer, 1993
- Chalcones: a new class of antimitotic agentsJournal of Medicinal Chemistry, 1990
- Uncoupling activities of chalcones and dihydrochalcones on isolated mitochondria from potato tubers and mung bean hypocotylsPhytochemistry, 1980