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The FEBS Journal|November 30, 2013
Structural and biochemical characterization of fructose-1,6/sedoheptulose-1,7-bisphosphatase from the cyanobacterium Synechocystis strain 6803Lingling Feng, Yao Sun, Hui Deng, et al.Organic & Biomolecular Chemistry|October 1, 2014
The design, synthesis and biological evaluation of novel thiamin diphosphate analog inhibitors against the pyruvate dehydrogenase multienzyme complex E1 from Escherichia coliLingling Feng, Junbo He, Haifeng He, et al.Journal of Agricultural and Food Chemistry|July 30, 2013
Structure-based design and synthesis of novel dual-target inhibitors against cyanobacterial fructose-1,6-bisphosphate aldolase and fructose-1,6-bisphosphataseDing Li, Xinya Han, Qidong Tu, et al.Bioorganic & Medicinal Chemistry|February 11, 2016
Synthesis and biological evaluation of novel inhibitors against 1,3,8-trihydroxynaphthalene reductase from Magnaporthe griseaHaifeng Chen, Xinya Han, Nian Qin, et al.Bioorganic & Medicinal Chemistry|December 18, 2017
Natural products as sources of new fungicides (IV): Synthesis and biological evaluation of isobutyrophenone analogs as potential inhibitors of class-II fructose-1,6-bisphosphate aldolaseDing Li, Tuong Thi Mai Luong, Wen-Jia Dan, et al.Journal of Chemical Information and Modeling|April 3, 2020
Cov_FB3D: A De Novo Covalent Drug Design Protocol Integrating the BA-SAMP Strategy and Machine-Learning-Based Synthetic Tractability EvaluationLin Wei, Wuqiang Wen, Li Rao, et al.Journal of Chemical Theory and Computation|May 31, 2019
Conformation Search Across Multiple-Level Potential-Energy Surfaces (CSAMP): A Strategy for Accurate Prediction of Protein-Ligand Binding StructuresLin Wei, Bo Chi, Yanliang Ren, et al.JACS Au|June 29, 2026
DeepDOX1: A Dual-Drive Framework Integrating Deep Learning and First-Principles Quantum Chemistry for Drug-Protein Affinity PredictionZheng Liu, Hao Sun, Yuliang Wang, et al.Bioorganic & Medicinal Chemistry|May 10, 2011
Specific inhibitions of annonaceous acetogenins on class II 3-hydroxy-3-methylglutaryl coenzyme A reductase from Streptococcus pneumoniaeLingling Feng, Li Zhou, Yao Sun, et al.Bioorganic & Medicinal Chemistry|December 18, 2014
Design, synthesis and evaluation of novel 5-phenylpyridin-2(1H)-one derivatives as potent reversible Bruton's tyrosine kinase inhibitorsXinge Zhao, Minhang Xin, Wei Huang, et al.Pageof 5