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Current Opinion in Drug Discovery & Development
|
February 1, 2006
The complexities inherent in attempts to decrease drug clearance by blocking sites of CYP-mediated metabolism
Michael B Fisher, Kirk R Henne, Jason Boer
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
April 28, 2010
Species-specific metabolism of SGX523 by aldehyde oxidase and the toxicological implications
Sharon Diamond, Jason Boer, Thomas P Maduskuie, et al.
ACS Medicinal Chemistry Letters
|
November 20, 2020
Biotransformation: Impact and Application of Metabolism in Drug Discovery
Julia Shanu-Wilson, Liam Evans, Stephen Wrigley, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 12, 2017
In Vitro Interactions of Epacadostat and its Major Metabolites with Human Efflux and Uptake Transporters: Implications for Pharmacokinetics and Drug Interactions
Qiang Zhang, Yan Zhang, Jason Boer, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
July 27, 2016
Roles of UGT, P450, and Gut Microbiota in the Metabolism of Epacadostat in Humans
Jason Boer, Ruth Young-Sciame, Fiona Lee, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
July 27, 2014
The Janus kinase 2 inhibitor fedratinib inhibits thiamine uptake: a putative mechanism for the onset of Wernicke's encephalopathy
Qiang Zhang, Yan Zhang, Sharon Diamond, et al.
Current Drug Metabolism
|
June 25, 2005
A comprehensive listing of bioactivation pathways of organic functional groups
Amit S Kalgutkar, Iain Gardner, R Scott Obach, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 12, 2009
Sulfoximine-substituted trifluoromethylpyrimidine analogs as inhibitors of proline-rich tyrosine kinase 2 (PYK2) show reduced hERG activity
Daniel P Walker, Michael P Zawistoski, Molly A McGlynn, et al.
Clinical Pharmacology and Therapeutics
|
December 11, 2023
Metabolite Bioanalysis in Drug Development: Recommendations from the IQ Consortium Metabolite Bioanalysis Working Group
Wenkui Li, Faye Vazvaei-Smith, Gordon Dear, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 16, 2011
A novel kinase inhibitor, INCB28060, blocks c-MET-dependent signaling, neoplastic activities, and cross-talk with EGFR and HER-3
Xiangdong Liu, Qian Wang, Gengjie Yang, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Current Opinion in Drug Discovery & Development
|
February 1, 2006
The complexities inherent in attempts to decrease drug clearance by blocking sites of CYP-mediated metabolism
Michael B Fisher, Kirk R Henne, Jason Boer
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
April 28, 2010
Species-specific metabolism of SGX523 by aldehyde oxidase and the toxicological implications
Sharon Diamond, Jason Boer, Thomas P Maduskuie, et al.
ACS Medicinal Chemistry Letters
|
November 20, 2020
Biotransformation: Impact and Application of Metabolism in Drug Discovery
Julia Shanu-Wilson, Liam Evans, Stephen Wrigley, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
March 12, 2017
In Vitro Interactions of Epacadostat and its Major Metabolites with Human Efflux and Uptake Transporters: Implications for Pharmacokinetics and Drug Interactions
Qiang Zhang, Yan Zhang, Jason Boer, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
July 27, 2016
Roles of UGT, P450, and Gut Microbiota in the Metabolism of Epacadostat in Humans
Jason Boer, Ruth Young-Sciame, Fiona Lee, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals
|
July 27, 2014
The Janus kinase 2 inhibitor fedratinib inhibits thiamine uptake: a putative mechanism for the onset of Wernicke's encephalopathy
Qiang Zhang, Yan Zhang, Sharon Diamond, et al.
Current Drug Metabolism
|
June 25, 2005
A comprehensive listing of bioactivation pathways of organic functional groups
Amit S Kalgutkar, Iain Gardner, R Scott Obach, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 12, 2009
Sulfoximine-substituted trifluoromethylpyrimidine analogs as inhibitors of proline-rich tyrosine kinase 2 (PYK2) show reduced hERG activity
Daniel P Walker, Michael P Zawistoski, Molly A McGlynn, et al.
Clinical Pharmacology and Therapeutics
|
December 11, 2023
Metabolite Bioanalysis in Drug Development: Recommendations from the IQ Consortium Metabolite Bioanalysis Working Group
Wenkui Li, Faye Vazvaei-Smith, Gordon Dear, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 16, 2011
A novel kinase inhibitor, INCB28060, blocks c-MET-dependent signaling, neoplastic activities, and cross-talk with EGFR and HER-3
Xiangdong Liu, Qian Wang, Gengjie Yang, et al.
Page
of 2