You Zhou

Expansion of the scaffold diversity for the development of highly selective butyrylcholinesterase (BChE) inhibitors: Discovery of new hits through the pharmacophore model generation, virtual screening and molecular dynamics simulation.

Q. Guo, Wenyuan Liu, F. Feng, 2019, Bioorganic chemistry.

Synthesis, cytotoxicity and topoisomerase II inhibitory activity of lomefloxacin derivatives.

Q. You, Haopeng Sun, Yuan Sun, 2013, Bioorganic & medicinal chemistry letters.

1 Synthesis and Structure-Activity Relationships of 2 Resorcinol Derivatives as Highly Potent Tyrosinase 3 Inhibitors 4

Q. Xia, Yao Chen, Hongyu Yang, 2018 .

Novel BuChE-IDO1 inhibitors from sertaconazole: Virtual screening, chemical optimization and molecular modeling studies.

Yijun Liu, Xin Lu, Haopeng Sun, 2020, Bioorganic & medicinal chemistry letters.

Discovery of a Selective 6-Hydroxy-1, 4-Diazepan-2-one Containing Butyrylcholinesterase Inhibitor by Virtual Screening and MM-GBSA Rescoring

Xin Lu, Haopeng Sun, K. H. Hong, 2020, Dose-response : a publication of International Hormesis Society.

Discovery of Selective Butyrylcholinesterase (BChE) Inhibitors through a Combination of Computational Studies and Biological Evaluations

Q. Xia, Xin Lu, Li Xu, 2019, Molecules.

Synthesis and activity of miconazole derivatives as dual BChE/IDO1 inhibitors for the treatment of Alzheimer's disease.

Wenyuan Liu, F. Feng, Yijun Liu, 2021, Future medicinal chemistry.

Investigation of multi-target-directed ligands (MTDLs) with butyrylcholinesterase (BuChE) and indoleamine 2,3-dioxygenase 1 (IDO1) inhibition: The design, synthesis of miconazole analogues targeting Alzheimer's disease.

F. Feng, Yaoyao Bian, Xin Lu, 2018, Bioorganic & medicinal chemistry.

Discovery and Design of Tricyclic Scaffolds as Protein Kinase CK2 (CK2) Inhibitors through a Combination of Shape-Based Virtual Screening and Structure-Based Molecular Modification

Fang Liu, Xiaoli Xu, Xiaowen Wu, 2013, J. Chem. Inf. Model..