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Peter M Fischer

Showing results (51-60 of 118) with videos related to

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Bioorganic & Medicinal Chemistry Letters|August 25, 2015
Discovery, synthesis and biochemical profiling of purine-2,6-dione derivatives as inhibitors of the human poly(A)-selective ribonuclease Caf1Gopal P Jadhav, Ishwinder Kaur, Maryati Maryati, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2002
Peptide inhibitors of CDK2-cyclin A that target the cyclin recruitment-site: structural variants of the C-terminal PheGail E Atkinson, Angela Cowan, Campbell McInnes, et al.
Cell Chemical Biology|July 19, 2018
The Meisenheimer Complex as a Paradigm in Drug Discovery: Reversible Covalent Inhibition through C67 of the ATP Binding Site of PLK1Russell J Pearson, David G Blake, Mokdad Mezna, et al.
Carcinogenesis|February 4, 2012
Small molecules that bind the Mdm2 RING stabilize and activate p53Patricia Roxburgh, Andreas K Hock, Michael P Dickens, et al.
AAPS Pharmscitech|June 1, 2017
Development of Cordycepin Formulations for Preclinical and Clinical StudiesJong Bong Lee, Cecilia Adrower, Chaolong Qin, et al.
Molecular Pharmacology|August 9, 2008
Role of key transmembrane residues in agonist and antagonist actions at the two conformations of the human beta1-adrenoceptorJillian G Baker, Richard G W Proudman, Nicola C Hawley, et al.
Molecules (Basel, Switzerland)|January 20, 2021
Strawberry Decreases Intraluminal and Intestinal Wall Hydrolysis of Testosterone UndecanoateAtheer Zgair, Yousaf Dawood, Suhaib M Ibrahem, et al.
Molecular Cancer Therapeutics|March 18, 2004
Cassette dosing pharmacokinetics of a library of 2,6,9-trisubstituted purine cyclin-dependent kinase 2 inhibitors prepared by parallel synthesisFlorence I Raynaud, Peter M Fischer, Bernard P Nutley, et al.
Journal of Medicinal Chemistry|April 26, 2013
Synthesis and in vitro and in vivo characterization of highly β1-selective β-adrenoceptor partial agonistsShailesh N Mistry, Jillian G Baker, Peter M Fischer, et al.
Journal of Medicinal Chemistry|March 8, 2011
Design, synthesis, and structure-activity relationship exploration of 1-substituted 4-aroyl-3-hydroxy-5-phenyl-1H-pyrrol-2(5H)-one analogues as inhibitors of the annexin A2-S100A10 protein interactionTummala R K Reddy, Chan Li, Xiaoxia Guo, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Bioorganic & Medicinal Chemistry Letters|August 25, 2015
Discovery, synthesis and biochemical profiling of purine-2,6-dione derivatives as inhibitors of the human poly(A)-selective ribonuclease Caf1Gopal P Jadhav, Ishwinder Kaur, Maryati Maryati, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2002
Peptide inhibitors of CDK2-cyclin A that target the cyclin recruitment-site: structural variants of the C-terminal PheGail E Atkinson, Angela Cowan, Campbell McInnes, et al.
Cell Chemical Biology|July 19, 2018
The Meisenheimer Complex as a Paradigm in Drug Discovery: Reversible Covalent Inhibition through C67 of the ATP Binding Site of PLK1Russell J Pearson, David G Blake, Mokdad Mezna, et al.
Carcinogenesis|February 4, 2012
Small molecules that bind the Mdm2 RING stabilize and activate p53Patricia Roxburgh, Andreas K Hock, Michael P Dickens, et al.
AAPS Pharmscitech|June 1, 2017
Development of Cordycepin Formulations for Preclinical and Clinical StudiesJong Bong Lee, Cecilia Adrower, Chaolong Qin, et al.
Molecular Pharmacology|August 9, 2008
Role of key transmembrane residues in agonist and antagonist actions at the two conformations of the human beta1-adrenoceptorJillian G Baker, Richard G W Proudman, Nicola C Hawley, et al.
Molecules (Basel, Switzerland)|January 20, 2021
Strawberry Decreases Intraluminal and Intestinal Wall Hydrolysis of Testosterone UndecanoateAtheer Zgair, Yousaf Dawood, Suhaib M Ibrahem, et al.
Molecular Cancer Therapeutics|March 18, 2004
Cassette dosing pharmacokinetics of a library of 2,6,9-trisubstituted purine cyclin-dependent kinase 2 inhibitors prepared by parallel synthesisFlorence I Raynaud, Peter M Fischer, Bernard P Nutley, et al.
Journal of Medicinal Chemistry|April 26, 2013
Synthesis and in vitro and in vivo characterization of highly β1-selective β-adrenoceptor partial agonistsShailesh N Mistry, Jillian G Baker, Peter M Fischer, et al.
Journal of Medicinal Chemistry|March 8, 2011
Design, synthesis, and structure-activity relationship exploration of 1-substituted 4-aroyl-3-hydroxy-5-phenyl-1H-pyrrol-2(5H)-one analogues as inhibitors of the annexin A2-S100A10 protein interactionTummala R K Reddy, Chan Li, Xiaoxia Guo, et al.
Pageof 12