Effects of anthrapyrazole antineoplastic agents on lipid peroxidation.
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Summary
All four drugs failed to decrease the rate of doxorubicin-stimulated NADPH oxidation at concentrations less than 50 microM, suggesting that inhibition of lipid peroxidation was not the result of diminished enzyme activity.
- Type
- article
- Published
- 1986-11-14
- Cited by
- 17
- References
- 14
- OpenAlex
- https://openalex.org/W2011668628
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:32460791
Keywords
Lipid peroxidation, Chemistry, Microsome, Biochemistry, Pharmacology
References
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- Anthrapyrazoles, a new class of intercalating agents with high-level, broad spectrum activity against murine tumors.
- Protein measurement with the Folin phenol reagent.
- Stimulation of mouse heart and liver microsomal lipid peroxidation by anthracycline anticancer drugs: characterization and effects of reactive oxygen scavengers.
- The anthracycline antineoplastic drugs.
- Solution chemistry studies of adriamycin--iron complexes present in vivo.
- Oxidative destruction of erythrocyte ghost membranes catalyzed by the doxorubicin-iron complex.
- Stimulation by adriamycin of rat heart and liver microsomal NADPH-dependent lipid peroxidation.
- In vitro DNA strand scission and inhibition of nucleic acid synthesis in L1210 leukemia cells by a new class of DNA complexers, the anthra[1,9-cd]pyrazol-6(2H)-ones (anthrapyrazoles).
- Oxidative destruction of DNA by the adriamycin-iron complex.
- Design, biochemical pharmacology, electrochemistry and tumour biology of anti-tumour anthrapyrazoles.
- Anthracycline antibiotic augmentation of microsomal electron transport and free radical formation.
Cited by
- Peroxidase induced metabolism and lipid peroxide scavenging by antitumor agents.
- The effect of the anthrapyrazole antitumour agent CI941 on rat liver microsome and cytochrome P-450 reductase mediated free radical processes. Inhibition of doxorubicin activation in vitro.
- Phase I study of high-dose piroxantrone with granulocyte colony-stimulating factor.
- Comparison of the chronic toxicity of piroxantrone, losoxantrone and doxorubicin in spontaneously hypertensive rats.
- Phase I pharmacokinetic study of DUP-937, a new anthrapyrazole
- The displacement of iron(III) from its complexes with the anticancer drugs piroxantrone and losoxantrone by the hydrolyzed form of the cardioprotective agent dexrazoxane.
- Status of new anthrapyrazole and pyrazoloacridine derivatives.
- The pharmacokinetics and toxicity of the anthrapyrazole anti-cancer drug CI-941 in the mouse: a guide for rational dose escalation in patients
- The ability of new formamidine sugar-modified derivatives of daunorubicin to stimulate free radical formation in three enzymatic systems: NADH dehydrogenase, NADPH cytochrome P450 reductase and xanthine oxidase.
- A multicenter phase II trial of losoxantrone (DuP-941) in hormone-refractory metastatic prostate cancer.
- Phase I pharmacokinetic and pharmacodynamic study of a new anthrapyrazole, CI-937 (DUP937).
- PHOTOSENSITIZATION OF NEOPLASTIC CELLS BY ANTHRAPYRAZOLES *
- The anthrapyrazoles: a new class of compounds with clinical activity in breast cancer.
- Navelbine and the anthrapyrazoles.
- Interaction of topoisomerase II-targeted anticancer agents with the doxorubicin cardioprotective drug dexrazoxane, and synthesis of a dexrazoxane analog
- Cellular and Molecular Pharmacology of the Anthrapyrazole Antitumour Agents
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