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Pigment Cell & Melanoma Research|January 30, 2009
BI-69A11-mediated inhibition of AKT leads to effective regression of xenograft melanomaSupriya Gaitonde, Surya K De, Marianna Tcherpakov, et al.Journal of Medicinal Chemistry|November 11, 2010
Design, synthesis, and structure-activity relationships of 3-ethynyl-1H-indazoles as inhibitors of the phosphatidylinositol 3-kinase signaling pathwayElisa Barile, Surya K De, Coby B Carlson, et al.Journal of Medicinal Chemistry|May 23, 2008
Development of paramagnetic probes for molecular recognition studies in protein kinasesJesus Vazquez, Surya K De, Li-Hsing Chen, et al.Journal of Medicinal Chemistry|August 6, 2011
Design and characterization of a potent and selective dual ATP- and substrate-competitive subnanomolar bidentate c-Jun N-terminal kinase (JNK) inhibitorJohn L Stebbins, Surya K De, Petra Pavlickova, et al.Bioorganic & Medicinal Chemistry|April 5, 2011
Design, synthesis, and structure-activity relationship studies of thiophene-3-carboxamide derivatives as dual inhibitors of the c-Jun N-terminal kinaseSurya K De, Elisa Barile, Vida Chen, et al.Cell Chemical Biology|February 16, 2017
Potent and Selective EphA4 Agonists for the Treatment of ALSBainan Wu, Surya K De, Anna Kulinich, et al.Chemistry & Biology|July 30, 2013
Structure-based design of covalent Siah inhibitorsJohn L Stebbins, Eugenio Santelli, Yongmei Feng, et al.ACS Chemical Biology|December 28, 2016
hBfl-1/hNOXA Interaction Studies Provide New Insights on the Role of Bfl-1 in Cancer Cell Resistance and for the Design of Novel Anticancer AgentsElisa Barile, Guya D Marconi, Surya K De, et al.Chemmedchem|November 10, 2012
Identification of small molecules that interfere with H1N1 influenza A viral replicationAngel Bottini, Surya K De, Bas J G Baaten, et al.Chemistry & Biology|July 14, 2015
Design and Characterization of Novel EphA2 Agonists for Targeted Delivery of Chemotherapy to Cancer CellsBainan Wu, Si Wang, Surya K De, et al.Pageof 6