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Human P450s involved in drug metabolism and the use of structural modelling for understanding substrate selectivity and binding affinity

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.

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Item Type: Article
Authors :
NameEmailORCID
Lewis, DFVd.lewis@surrey.ac.ukUNSPECIFIED
Ito, YUNSPECIFIEDUNSPECIFIED
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
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/824258

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