Quantitative structure-activity relationships (QSARs) in CYP3A4 inhibitors: The importance of lipophilic character and hydrogen bonding
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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.
Full text not available from this repository.| Item Type: | Article | ||||||||||||
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| Divisions : | Surrey research (other units) | ||||||||||||
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| Date : | 1 April 2006 | ||||||||||||
| DOI : | 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 | ||||||||||||
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| Depositing User : | Symplectic Elements | ||||||||||||
| Date Deposited : | 17 May 2017 09:34 | ||||||||||||
| Last Modified : | 24 Jan 2020 17:11 | ||||||||||||
| URI: | http://epubs.surrey.ac.uk/id/eprint/824251 |
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