Quantitative structure-activity relationships (QSARs) for inhibitors and substrates of CYP2B enzymes: importance of compound lipophilicity in explanation of potency differences
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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.
Full text not available from this repository.| Item Type: | Article | ||||||||||||
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| Date : | 1 October 2010 | ||||||||||||
| DOI : | 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 | ||||||||||||
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| 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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