Quantitative structure-activity relationships (QSARs) for inhibitors and substrates of CYP2B enzymes: importance of compound lipophilicity in explanation of potency differences

Lewis, DFV, Ito, Y and Lake, BG (2010) Quantitative structure-activity relationships (QSARs) for inhibitors and substrates of CYP2B enzymes: importance of compound lipophilicity in explanation of potency differences JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 25 (5). pp. 679-684.

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Item Type:	Article
Authors :	Name Email ORCID Lewis, DFV d.lewis@surrey.ac.uk UNSPECIFIED Ito, Y UNSPECIFIED UNSPECIFIED Lake, BG UNSPECIFIED UNSPECIFIED
Date :	1 October 2010
Identification Number :	https://doi.org/10.3109/14756360903514149
Uncontrolled Keywords :	Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Chemistry, Medicinal, Pharmacology & Pharmacy, BIOCHEMISTRY & MOLECULAR BIOLOGY, CHEMISTRY, MEDICINAL, Cytochromes P450, QSARs, Lipophilicity, Enzyme Inhibition, DRUG-METABOLISM, PARTITION-COEFFICIENTS, CYTOCHROMES P450, 3D DESCRIPTORS, IN-VITRO, BINDING, 2D
Related URLs :	Author
Depositing User :	Symplectic Elements
Date Deposited :	17 May 2017 09:34
Last Modified :	17 May 2017 09:34
URI:	http://epubs.surrey.ac.uk/id/eprint/824267

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