Human P450s involved in drug metabolism and the use of structural modelling for understanding substrate selectivity and binding affinity
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Lewis, DFV and Ito, Y (2009) Human P450s involved in drug metabolism and the use of structural modelling for understanding substrate selectivity and binding affinity XENOBIOTICA, 39 (8). pp. 625-635.
Full text not available from this repository.| Item Type: | Article | |||||||||
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| Date : | 1 January 2009 | |||||||||
| Identification Number : | https://doi.org/10.1080/00498250903000255 | |||||||||
| Uncontrolled Keywords : | Science & Technology, Life Sciences & Biomedicine, Pharmacology & Pharmacy, Toxicology, PHARMACOLOGY & PHARMACY, TOXICOLOGY, Human cytochrome P450s, substrate selectivity, binding affinity, HUMAN CYTOCHROMES P450, CHEMICAL TOXICOLOGY, ANGSTROM RESOLUTION, AUTOMATED DOCKING, CRYSTAL-STRUCTURE, FAMILY ENZYMES, K-M, LIPOPHILICITY, QSARS, 3A4 | |||||||||
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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/824258 |
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