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Bioorganic & Medicinal Chemistry|March 14, 2009
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitorsSurya K De, Li-Hsing Chen, John L Stebbins, et al.Journal of Medicinal Chemistry|March 11, 2009
Design, synthesis, and structure-activity relationship of substrate competitive, selective, and in vivo active triazole and thiadiazole inhibitors of the c-Jun N-terminal kinaseSurya K De, John L Stebbins, Li-Hsing Chen, et al.Chemical Biology & Drug Design|July 28, 2011
A disalicylic acid-furanyl derivative inhibits ephrin binding to a subset of Eph receptorsRoberta Noberini, Surya K De, Ziming Zhang, et al.Plos One|October 2, 2012
Functional specialization in proline biosynthesis of melanomaJessica De Ingeniis, Boris Ratnikov, Adam D Richardson, et al.Pigment Cell & Melanoma Research|May 20, 2011
Effective inhibition of melanoma by BI-69A11 is mediated by dual targeting of the AKT and NF-κB pathwaysYongmei Feng, Elisa Barile, Surya K De, et al.Proceedings of the National Academy of Sciences of the United States of America|October 17, 2008
Identification of a new JNK inhibitor targeting the JNK-JIP interaction siteJohn L Stebbins, Surya K De, Thomas Machleidt, et al.Bioorganic & Medicinal Chemistry|January 5, 2010
Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitorsSurya K De, Vida Chen, John L Stebbins, et al.Oncotarget|March 10, 2016
Therapy of pancreatic cancer via an EphA2 receptor-targeted delivery of gemcitabineBridget A Quinn, Si Wang, Elisa Barile, et al.Cell Reports|September 23, 2016
Control of Paneth Cell Fate, Intestinal Inflammation, and Tumorigenesis by PKCλ/ιYuki Nakanishi, Miguel Reina-Campos, Naoko Nakanishi, et al.Pigment Cell & Melanoma Research|October 6, 2012
Inhibition of melanoma development in the Nras((Q61K)) ::Ink4a(-/-) mouse model by the small molecule BI-69A11Yongmei Feng, Eric Lau, Marzia Scortegagna, et al.Pageof 6