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Oncotarget|October 27, 2015
Flavokawain A induces deNEDDylation and Skp2 degradation leading to inhibition of tumorigenesis and cancer progression in the TRAMP transgenic mouse modelXuesen Li, Noriko N Yokoyama, Saiyang Zhang, et al.Journal of Biomolecular Structure & Dynamics|September 4, 2018
Probing the binding mechanism of substituted pyridine derivatives as effective and selective lysine-specific demethylase 1 inhibitors using 3D-QSAR, molecular docking and molecular dynamics simulationsZhi-Zheng Wang, Jing Yang, Xu-Dong Sun, et al.Steroids|August 6, 2013
Design and synthesis of novel D-ring fused steroidal heterocyclesBao-Le Zhang, En Zhang, Lu-Ping Pang, et al.Molecular and Cellular Biochemistry|July 17, 2020
OP16 induces deadly autophagy and apoptosis of cells by inhibiting Akt in esophageal squamous cell carcinomaGuiqin Hou, Ang Jia, Li Yang, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 28, 2018
FLI-06 suppresses proliferation, induces apoptosis and cell cycle arrest by targeting LSD1 and Notch pathway in esophageal squamous cell carcinoma cellsZhaoming Lu, Yandan Ren, Mengying Zhang, et al.Journal of Hematology & Oncology|April 8, 2021
Targeting neddylation E2s: a novel therapeutic strategy in cancerYi-Chao Zheng, Yan-Jia Guo, Bo Wang, et al.European Journal of Medicinal Chemistry|July 19, 2020
Discovery of tofacitinib derivatives as orally active antitumor agents based on the scaffold hybridization strategyXiao-Jing Shi, Shuai Wang, Xiao-Jing Li, et al.European Journal of Pharmacology|December 26, 2021
Discovery of the antitumor activities of a potent DCN1 inhibitor compound 383 targeting LSD1 in gastric cancerZan Song, Ke Gao, Moges Dessale Asmamaw, et al.European Journal of Medicinal Chemistry|October 8, 2021
Discovery of a cinnamyl piperidine derivative as new neddylation inhibitor for gastric cancer treatmentBo Wang, Qiu-Hua Zhang, Xiao-Jing Li, et al.Bioorganic & Medicinal Chemistry Letters|October 18, 2017
Discovery of tranylcypromine analogs with an acylhydrazone substituent as LSD1 inactivators: Design, synthesis and their biological evaluationKai Sun, Jia-Di Peng, Feng-Zhi Suo, et al.Pageof 34