HIGH CONTENT SCREENING OF POTENTIAL DRUG COMPOUNDS TO DETECT MODULATORY EFFECTS ON CYTOCHROME P450 (CYP) ENZYMES
- Authors: Klyushova L.S1
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Affiliations:
- Institute of Molecular Biology and Biophysics - subdivision of FRC FTM
- Issue: Vol 15, No 3S (2020)
- Pages: 51-52
- Section: Articles
- URL: https://genescells.ru/2313-1829/article/view/122639
- DOI: https://doi.org/10.23868/gc122639
- ID: 122639
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Abstract
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About the authors
L. S Klyushova
Institute of Molecular Biology and Biophysics - subdivision of FRC FTM
Email: klyushovals@mail.ru
Novosibirsk, Russie
References
- Zanger U.M., Schwab M. Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation. PharmacolTher. 2013; 138 (1): 103-141.
- Lolodi O.et al. Differential Regulation of CYP3A4 and CY-P3A5 and Its Implication in Drug Discovery. Curr Drug Metab. 2017; 18(12): 1095-1105.
- Eremina J. A.et al. Mixed-ligand copper(ll) complexes with tetrazole derivatives and 2,2'-bipyridine, 1,10-phenanthroline: synthesis, structure and cytotoxic activity. Inorg. Chim. Acta. 2019; 487: 138-144.
- Mattiazzi U.M.et al. High-Content Screening for Quantitative Cell Biology. Trends Cell Biol. 2016; 26(8): 598-611.