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Xenobiotica
the fate of foreign compounds in biological systems
Volume 24, 1994 - Issue 9
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Original Article

Inhibition of rat hepatic aryl hydrocarbon hydroxylase activity by a series of 7-hydroxy coumarins: QSAR studies

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Pages 829-838 | Received 20 May 1994, Published online: 27 Aug 2009

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David F.V. Lewis & Maurice Dickins. (2001) Quantitative Structure-Activity Relationships (QSARs) Within Series of Inhibitors for Mammalian Cytochromes P450 (CYPs). Journal of Enzyme Inhibition 16:4, pages 321-330.
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D. F. V. Lewis, C. Ioannides & D. V. Parke. (1998) An Improved and Updated Version of the Compact Procedure for the Evaluation of P450-Mediated Chemical Activation. Drug Metabolism Reviews 30:4, pages 709-737.
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Mohsen Shahlaei & Zohreh Nazari. (2013) Prediction of glucagon receptor antagonist activities of some substituted imidazoles using combined radial basis function neural network and density functional theory. Medicinal Chemistry Research 23:6, pages 2744-2756.
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Mohsen Shahlaei & Zohreh Nazari. (2013) Computational neural network analysis of the affinity of 2-pyridyl-3,5-diaryl pyrroles analogs for the human glucagon receptor using density functional theory. Medicinal Chemistry Research 23:4, pages 2046-2061.
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Nadia Hanafy Metwally & Sabry El-Taher. (2011) Synthesis, Theoretical Study, and Antimicrobial Activity of Novel Polysubstituted Thiazoles. HETEROCYCLES 83:5, pages 1029.
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V. S. Moskvina & V. P. Khilya. (2008) Synthesis of pyrano[2,3-f]chromen-2,8-diones and pyrano[3,2-g]chromen-2,8-diones based on o-hydroxyformyl(acyl)neoflavonoids. Chemistry of Natural Compounds 44:1, pages 16-23.
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Andre Kimura Okamoto, Anderson Coser Gaudio, Alberto dos Santos Marques & Yuji Takahata. (2005) QSAR study of inibition by coumarins of IQ induced mutation in S. typhimurium TA98. Journal of Molecular Structure: THEOCHEM 725:1-3, pages 231-238.
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David F. V. Lewis. (2003) Quantitative structure–activity relationships (QSARs) within the cytochrome P450 system: QSARs describing substrate binding, inhibition and induction of P450s. InflammoPharmacology 11:1, pages 43-73.
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David F?V Lewis. (2001) COMPACT: a structural approach to the modelling of cytochromes P450 and their interactions with xenobiotics. Journal of Chemical Technology & Biotechnology 76:3, pages 237-244.
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David F.V. Lewis, Brian G. Lake, Stephen G. George, Maurice Dickins, Peter J. Eddershaw, Michael H. Tarbit, Alan P. Beresford, Peter S. Goldfarb & F.Peter Guengerich. (1999) Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102. Toxicology 139:1-2, pages 53-79.
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T.B. Adams, D.B. Greer, J. Doull, I.C. Munro, P. Newberne, P.S. Portoghese, R.L. Smith, B.M. Wagner, C.S. Weil, L.A. Woods & R.A. Ford. (1998) The FEMA GRAS Assessment of Lactones Used as Flavour Ingredients. Food and Chemical Toxicology 36:4, pages 249-278.
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D. F. V. Lewis. 1997. Food Chemical Risk Analysis. Food Chemical Risk Analysis 163 194 .
Mati Karelson, Victor S. Lobanov & Alan R. Katritzky. (1996) Quantum-Chemical Descriptors in QSAR/QSPR Studies. Chemical Reviews 96:3, pages 1027-1044.
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D V Parke. (1994) The cytochromes P450 and mechanisms of chemical carcinogenesis.. Environmental Health Perspectives 102:10, pages 852-853.
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