CYP3A4 overexpression enhances apoptosis induced by anticancer agent imidazoacridinone C-1311, but does not change the metabolism of C-1311 in CHO cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Pharmacology,General Medicine
Link
http://www.nature.com/articles/aps2013132.pdf
Reference54 articles.
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2. Guengerich FP . Cytochrome P450s and other enzymes in drug metabolism and toxicity. AAPS J 2006; 8: 101–11.
3. Henderson CJ, Otto DM, Carrie D, Magnuson MA, McLaren AW, Rosewell I, et al. Inactivation of the hepatic cytochrome P450 system by conditional deletion of hepatic cytochrome P450 reductase. J Biol Chem 2003; 278: 13480–6.
4. Cholody WM, Martelli S, Paradziej-Lukowicz J, Konopa J . 5-[(Aminoalkyl)amino]imidazo[4,5,1-de]acridin-6-ones as a novel class of antineoplastic agents. Synthesis and biological activity. J Med Chem 1990; 33: 49–52.
5. Cholody WM, Martelli S, Konopa J . Chromophore-modified antineoplastic imidazoacridinones. Synthesis and activity against murine leukemias. J Med Chem 1992; 35: 378–82.
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