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Oncology Reports|April 4, 2025
[Retracted] (‑)‑β‑hydrastine suppresses the proliferation and invasion of human lung adenocarcinoma cells by inhibiting PAK4 kinase activityBingyu Guo, Xiaodong Li, Shuai Song, et al.Journal of Molecular Graphics & Modelling|October 22, 2018
Computational investigation of the antagonism effect towards GluN2B-Containing NMDA receptor: Combined ligand-based and target-based approachChao Ma, Baichun Hu, Linkui Zhang, et al.Expert Opinion on Therapeutic Patents|August 9, 2021
Drug discovery targeting p21-activated kinase 4 (PAK4): a patent reviewHanxun Wang, Peilu Song, Yinli Gao, et al.Oncology Reports|January 29, 2016
(-)-β-hydrastine suppresses the proliferation and invasion of human lung adenocarcinoma cells by inhibiting PAK4 kinase activityBingyu Guo, Xiaodong Li, Shuai Song, et al.Chirality|October 12, 2013
Bidirectional chiral inversion of trantinterol enantiomers after separate doses to ratsFeng Qin, Xintao Wang, Lijuan Jing, et al.Chirality|March 18, 2015
Determination of trantinterol enantiomers in human plasma by high-performance liquid chromatography - tandem mass spectrometry using vancomycin chiral stationary phase and solid phase extraction and stereoselective pharmacokinetic applicationFeng Qin, Yanjuan Wang, Lijuan Wang, et al.Organic Letters|July 17, 2025
Unlocking the Potential of Ynamide as a Promoter in Copper(II)-Catalyzed O-GlycosylationHanyang Sun, Zixuan Liu, Bin Bai, et al.The Analyst|June 16, 2015
Metal-organic framework MIL-101(Cr) as a sorbent of porous membrane-protected micro-solid-phase extraction for the analysis of six phthalate esters from drinking water: a combination of experimental and computational studyTing Wang, Jian Wang, Conglu Zhang, et al.International Journal of Molecular Sciences|December 24, 2021
Synthesis, Molecular Docking Analysis, and Biological Evaluations of Saccharide-Modified Sulfonamides as Carbonic Anhydrase IX InhibitorsZuopeng Zhang, Huali Yang, Ye Zhong, et al.Bioorganic Chemistry|April 11, 2022
Discovery of benzo[d]isothiazole derivatives as novel scaffold inhibitors targeting the programmed cell death-1/programmed cell death-ligand 1 (PD-1/PD-L1) interaction through "ring fusion" strategyYinli Gao, Hanxun Wang, Lanlan Shen, et al.Pageof 32