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Jeremy Murray

Showing results (21-30 of 65) with videos related to

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Nature Chemical Biology|June 12, 2012
Allosteric peptides bind a caspase zymogen and mediate caspase tetramerizationKaren Stanger, Micah Steffek, Lijuan Zhou, et al.
ACS Medicinal Chemistry Letters|January 17, 2024
Structure-Based Design and Evaluation of Reversible KRAS G13D InhibitorsChristian Nilewski, Sharada Labadie, Binqing Wei, et al.
Chemistry & Biology|August 2, 2011
The development of peptide-based tools for the analysis of angiogenesisAnna Fedorova, Kerry Zobel, Herman S Gill, et al.
Cell Death and Differentiation|August 13, 2016
Coordinated ubiquitination and phosphorylation of RIP1 regulates necroptotic cell deathM Cristina de Almagro, Tatiana Goncharov, Anita Izrael-Tomasevic, et al.
International Journal of Molecular Sciences|March 27, 2025
Integrated Transcriptomic and Metabolomic Analysis Reveals Tissue-Specific Flavonoid Biosynthesis and MYB-Mediated Regulation of UGT71A1 in <i>Panax quinquefolius</i>Yumeng Wang, Jiaxin Zhang, Ping Wang, et al.
Journal of Medicinal Chemistry|September 23, 2011
Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinaseVito Guagnano, Pascal Furet, Carsten Spanka, et al.
Bioorganic & Medicinal Chemistry Letters|October 14, 2015
Discovery of 3,5-substituted 6-azaindazoles as potent pan-Pim inhibitorsHuiyong Hu, Xiaojing Wang, Grace Ka Yan Chan, et al.
Chemmedchem|November 22, 2013
Tailoring small molecules for an allosteric site on procaspase-6Jeremy Murray, Anthony M Giannetti, Micah Steffek, et al.
Journal of Medicinal Chemistry|April 27, 2017
Discovery of 5-Azaindazole (GNE-955) as a Potent Pan-Pim Inhibitor with Optimized BioavailabilityXiaojing Wang, Aleksandr Kolesnikov, Suzanne Tay, et al.
Bioorganic & Medicinal Chemistry Letters|December 26, 2012
Cis-amide isosteric replacement in thienobenzoxepin inhibitors of PI3-kinaseSteven T Staben, Nicole Blaquiere, Vickie Tsui, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Nature Chemical Biology|June 12, 2012
Allosteric peptides bind a caspase zymogen and mediate caspase tetramerizationKaren Stanger, Micah Steffek, Lijuan Zhou, et al.
ACS Medicinal Chemistry Letters|January 17, 2024
Structure-Based Design and Evaluation of Reversible KRAS G13D InhibitorsChristian Nilewski, Sharada Labadie, Binqing Wei, et al.
Chemistry & Biology|August 2, 2011
The development of peptide-based tools for the analysis of angiogenesisAnna Fedorova, Kerry Zobel, Herman S Gill, et al.
Cell Death and Differentiation|August 13, 2016
Coordinated ubiquitination and phosphorylation of RIP1 regulates necroptotic cell deathM Cristina de Almagro, Tatiana Goncharov, Anita Izrael-Tomasevic, et al.
International Journal of Molecular Sciences|March 27, 2025
Integrated Transcriptomic and Metabolomic Analysis Reveals Tissue-Specific Flavonoid Biosynthesis and MYB-Mediated Regulation of UGT71A1 in <i>Panax quinquefolius</i>Yumeng Wang, Jiaxin Zhang, Ping Wang, et al.
Journal of Medicinal Chemistry|September 23, 2011
Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinaseVito Guagnano, Pascal Furet, Carsten Spanka, et al.
Bioorganic & Medicinal Chemistry Letters|October 14, 2015
Discovery of 3,5-substituted 6-azaindazoles as potent pan-Pim inhibitorsHuiyong Hu, Xiaojing Wang, Grace Ka Yan Chan, et al.
Chemmedchem|November 22, 2013
Tailoring small molecules for an allosteric site on procaspase-6Jeremy Murray, Anthony M Giannetti, Micah Steffek, et al.
Journal of Medicinal Chemistry|April 27, 2017
Discovery of 5-Azaindazole (GNE-955) as a Potent Pan-Pim Inhibitor with Optimized BioavailabilityXiaojing Wang, Aleksandr Kolesnikov, Suzanne Tay, et al.
Bioorganic & Medicinal Chemistry Letters|December 26, 2012
Cis-amide isosteric replacement in thienobenzoxepin inhibitors of PI3-kinaseSteven T Staben, Nicole Blaquiere, Vickie Tsui, et al.
Pageof 7