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Quantitative structure-activity relationships (QSARs) in CYP3A4 inhibitors: The importance of lipophilic character and hydrogen bonding

Lewis, DFV, Lake, BG and Dickns, M (2006) Quantitative structure-activity relationships (QSARs) in CYP3A4 inhibitors: The importance of lipophilic character and hydrogen bonding JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 21 (2). pp. 127-132.

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Item Type: Article
Authors :
NameEmailORCID
Lewis, DFVd.lewis@surrey.ac.ukUNSPECIFIED
Lake, BGUNSPECIFIEDUNSPECIFIED
Dickns, MUNSPECIFIEDUNSPECIFIED
Date : 1 April 2006
Identification Number : https://doi.org/10.1080/14756360500532747
Uncontrolled Keywords : Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Chemistry, Medicinal, Pharmacology & Pharmacy, BIOCHEMISTRY & MOLECULAR BIOLOGY, CHEMISTRY, MEDICINAL, CYP3A4, inhibition, partition coefficient, statins, QSAR, HUMAN CYTOCHROMES P450, DRUG-METABOLISM, IN-VITRO, ENZYMES
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/824251

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