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Quantitative structure-activity relationships (QSARs) in inhibitors of various cytochromes P450: The importance of compound lipophilicity

Lewis, DFV, Lake, BG and Dickins, M (2007) Quantitative structure-activity relationships (QSARs) in inhibitors of various cytochromes P450: The importance of compound lipophilicity JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 22 (1). pp. 1-6.

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Item Type: Article
Authors :
NameEmailORCID
Lewis, DFVd.lewis@surrey.ac.ukUNSPECIFIED
Lake, BGUNSPECIFIEDUNSPECIFIED
Dickins, MUNSPECIFIEDUNSPECIFIED
Date : 1 February 2007
Identification Number : 10.1080/14756360600952183
Uncontrolled Keywords : Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Chemistry, Medicinal, Pharmacology & Pharmacy, BIOCHEMISTRY & MOLECULAR BIOLOGY, CHEMISTRY, MEDICINAL, cytochrome P450, inhibitors, QSAR, lipophilicity, CYP2C5 CRYSTALLOGRAPHIC TEMPLATE, SUBSTRATE INTERACTIONS, METABOLISM, HOMOLOGY, BINDING, ENZYMES, CYP3A4
Related URLs :
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/824243

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