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Bioorganic Chemistry|April 7, 2019
Sanggenon O induced apoptosis of A549 cells is counterbalanced by protective autophagyZhong-Rui Li, Ting Ma, Yan-Jia Guo, et al.Journal of Medicinal Chemistry|December 23, 2021
Discovery of Potent and Selective 2-(Benzylthio)pyrimidine-based DCN1-UBC12 Inhibitors for Anticardiac Fibrotic EffectsZhang-Xu He, Qi An, Bo Wei, et al.Acta Pharmaceutica Sinica. B|August 15, 2022
Preclinical studies of the triazolo[1,5-a]pyrimidine derivative WS-716 as a highly potent, specific and orally active P-glycoprotein (P-gp) inhibitorSai-Qi Wang, Qiu-Xu Teng, Shuai Wang, et al.International Journal of Biological Macromolecules|January 15, 2023
Curriculum vitae of HDAC6 in solid tumorsYi-Chao Zheng, Hui-Qin Kang, Bo Wang, et al.European Journal of Medicinal Chemistry|August 4, 2014
Synthesis and anticancer activities of novel 1,2,4-triazolo[3,4-a]phthalazine derivativesDeng-Qi Xue, Xu-Yao Zhang, Chao-Jie Wang, et al.European Journal of Medicinal Chemistry|August 2, 2017
Discovery of 5,6-diaryl-1,2,4-triazines hybrids as potential apoptosis inducersDong-Jun Fu, Jian Song, Yu-Hui Hou, et al.European Journal of Medicinal Chemistry|December 31, 2016
Design and synthesis of formononetin-dithiocarbamate hybrids that inhibit growth and migration of PC-3 cells via MAPK/Wnt signaling pathwaysDong-Jun Fu, Li Zhang, Jian Song, et al.Scientific Reports|October 8, 2017
Structure-Activity Relationship Studies of β-Lactam-azide Analogues as Orally Active Antitumor Agents Targeting the Tubulin Colchicine SiteDong-Jun Fu, Ling Fu, Ying-Chao Liu, et al.Pharmacological Research|June 3, 2017
LPE-1, an orally active pyrimidine derivative, inhibits growth and mobility of human esophageal cancers by targeting LSD1Bo Wang, Bing Zhao, Lu-Ping Pang, et al.Journal of Medicinal Chemistry|October 18, 2013
Triazole-dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migrationYi-Chao Zheng, Ying-Chao Duan, Jin-Lian Ma, et al.Pageof 34