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Campbell McInnes

Showing results (41-50 of 61) with videos related to

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Journal of Medicinal Chemistry|December 17, 2008
Synthesis and evaluation of novel inhibitors of Pim-1 and Pim-2 protein kinasesZuping Xia, Christian Knaak, Jian Ma, et al.
Chembiochem : a European Journal of Chemical Biology|October 20, 2006
REPLACE: a strategy for iterative design of cyclin-binding groove inhibitorsMartin J I Andrews, George Kontopidis, Campbell McInnes, et al.
ACS Chemical Biology|May 23, 2012
Calpain 10 homology modeling with CYGAK and increased lipophilicity leads to greater potency and efficacy in cellsMatthew A Smith, Campbell McInnes, Ryan M Whitaker, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2005
Structural and biochemical studies of human proliferating cell nuclear antigen complexes provide a rationale for cyclin association and inhibitor designGeorge Kontopidis, Su-Ying Wu, Daniella I Zheleva, et al.
Molecular Cancer Therapeutics|August 1, 2012
Targeting subcellular localization through the polo-box domain: non-ATP competitive inhibitors recapitulate a PLK1 phenotypeCampbell McInnes, Kara Estes, Merissa Baxter, et al.
Chemistry & Biology|February 24, 2006
Differential binding of inhibitors to active and inactive CDK2 provides insights for drug designGeorge Kontopidis, Campbell McInnes, Sravan R Pandalaneni, et al.
Nature Chemical Biology|October 10, 2006
Inhibitors of Polo-like kinase reveal roles in spindle-pole maintenanceCampbell McInnes, Aveek Mazumdar, Mokdad Mezna, et al.
Journal of Medicinal Chemistry|February 3, 2022
A Selective and Orally Bioavailable Quinoline-6-Carbonitrile-Based Inhibitor of CDK8/19 Mediator Kinase with Tumor-Enriched PharmacokineticsLi Zhang, Chen Cheng, Jing Li, et al.
Chemistry & Biology|May 5, 2004
Structural determinants of CDK4 inhibition and design of selective ATP competitive inhibitorsCampbell McInnes, Shudong Wang, Sian Anderson, et al.
Bioorganic & Medicinal Chemistry Letters|July 21, 2004
Synthesis and biological activity of 2-anilino-4-(1H-pyrrol-3-yl) pyrimidine CDK inhibitorsShudong Wang, Gavin Wood, Christopher Meades, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Journal of Medicinal Chemistry|December 17, 2008
Synthesis and evaluation of novel inhibitors of Pim-1 and Pim-2 protein kinasesZuping Xia, Christian Knaak, Jian Ma, et al.
Chembiochem : a European Journal of Chemical Biology|October 20, 2006
REPLACE: a strategy for iterative design of cyclin-binding groove inhibitorsMartin J I Andrews, George Kontopidis, Campbell McInnes, et al.
ACS Chemical Biology|May 23, 2012
Calpain 10 homology modeling with CYGAK and increased lipophilicity leads to greater potency and efficacy in cellsMatthew A Smith, Campbell McInnes, Ryan M Whitaker, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2005
Structural and biochemical studies of human proliferating cell nuclear antigen complexes provide a rationale for cyclin association and inhibitor designGeorge Kontopidis, Su-Ying Wu, Daniella I Zheleva, et al.
Molecular Cancer Therapeutics|August 1, 2012
Targeting subcellular localization through the polo-box domain: non-ATP competitive inhibitors recapitulate a PLK1 phenotypeCampbell McInnes, Kara Estes, Merissa Baxter, et al.
Chemistry & Biology|February 24, 2006
Differential binding of inhibitors to active and inactive CDK2 provides insights for drug designGeorge Kontopidis, Campbell McInnes, Sravan R Pandalaneni, et al.
Nature Chemical Biology|October 10, 2006
Inhibitors of Polo-like kinase reveal roles in spindle-pole maintenanceCampbell McInnes, Aveek Mazumdar, Mokdad Mezna, et al.
Journal of Medicinal Chemistry|February 3, 2022
A Selective and Orally Bioavailable Quinoline-6-Carbonitrile-Based Inhibitor of CDK8/19 Mediator Kinase with Tumor-Enriched PharmacokineticsLi Zhang, Chen Cheng, Jing Li, et al.
Chemistry & Biology|May 5, 2004
Structural determinants of CDK4 inhibition and design of selective ATP competitive inhibitorsCampbell McInnes, Shudong Wang, Sian Anderson, et al.
Bioorganic & Medicinal Chemistry Letters|July 21, 2004
Synthesis and biological activity of 2-anilino-4-(1H-pyrrol-3-yl) pyrimidine CDK inhibitorsShudong Wang, Gavin Wood, Christopher Meades, et al.
Pageof 7