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Mark C Wenlock

Showing results (1-10 of 12) with videos related to

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Molecular Pharmaceutics|January 12, 2013
In silico physicochemical parameter predictionsMark C Wenlock, Patrick Barton
Journal of Computer-Aided Molecular Design|June 10, 2015
Interpreting physicochemical experimental data setsNicola Colclough, Mark C Wenlock
Journal of Chemical Information and Modeling|November 19, 2014
How experimental errors influence drug metabolism and pharmacokinetic QSAR/QSPR modelsMark C Wenlock, Lars A Carlsson
Bioorganic & Medicinal Chemistry Letters|May 24, 2011
Lipophilicity of acidic compounds: impact of ion pair partitioning on drug designMark C Wenlock, Patrick Barton, Tim Luker
Journal of Pharmaceutical and Biomedical Analysis|March 5, 2011
A kinetic method for the determination of plasma protein binding of compounds unstable in plasma: Specific application to enalaprilMark C Wenlock, Patrick Barton, Rupert P Austin
Journal of Laboratory Automation|July 19, 2011
A highly automated assay for determining the aqueous equilibrium solubility of drug discovery compoundsMark C Wenlock, Rupert P Austin, Tim Potter, et al.
Journal of Biomolecular Screening|February 24, 2011
A method for measuring the lipophilicity of compounds in mixtures of 10Mark C Wenlock, Tim Potter, Patrick Barton, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 16, 2002
The influence of nonspecific microsomal binding on apparent intrinsic clearance, and its prediction from physicochemical propertiesRupert P Austin, Patrick Barton, Scott L Cockroft, et al.
Journal of Medicinal Chemistry|March 21, 2003
A comparison of physiochemical property profiles of development and marketed oral drugsMark C Wenlock, Rupert P Austin, Patrick Barton, et al.
Pharmaceutical Research|September 24, 2005
The thermodynamics of the partitioning of ionizing molecules between aqueous buffers and phospholipid membranesRupert P Austin, Patrick Barton, Andrew M Davis, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Molecular Pharmaceutics|January 12, 2013
In silico physicochemical parameter predictionsMark C Wenlock, Patrick Barton
Journal of Computer-Aided Molecular Design|June 10, 2015
Interpreting physicochemical experimental data setsNicola Colclough, Mark C Wenlock
Journal of Chemical Information and Modeling|November 19, 2014
How experimental errors influence drug metabolism and pharmacokinetic QSAR/QSPR modelsMark C Wenlock, Lars A Carlsson
Bioorganic & Medicinal Chemistry Letters|May 24, 2011
Lipophilicity of acidic compounds: impact of ion pair partitioning on drug designMark C Wenlock, Patrick Barton, Tim Luker
Journal of Pharmaceutical and Biomedical Analysis|March 5, 2011
A kinetic method for the determination of plasma protein binding of compounds unstable in plasma: Specific application to enalaprilMark C Wenlock, Patrick Barton, Rupert P Austin
Journal of Laboratory Automation|July 19, 2011
A highly automated assay for determining the aqueous equilibrium solubility of drug discovery compoundsMark C Wenlock, Rupert P Austin, Tim Potter, et al.
Journal of Biomolecular Screening|February 24, 2011
A method for measuring the lipophilicity of compounds in mixtures of 10Mark C Wenlock, Tim Potter, Patrick Barton, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 16, 2002
The influence of nonspecific microsomal binding on apparent intrinsic clearance, and its prediction from physicochemical propertiesRupert P Austin, Patrick Barton, Scott L Cockroft, et al.
Journal of Medicinal Chemistry|March 21, 2003
A comparison of physiochemical property profiles of development and marketed oral drugsMark C Wenlock, Rupert P Austin, Patrick Barton, et al.
Pharmaceutical Research|September 24, 2005
The thermodynamics of the partitioning of ionizing molecules between aqueous buffers and phospholipid membranesRupert P Austin, Patrick Barton, Andrew M Davis, et al.
Pageof 2