BETA: Related publications
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| Yan G, Hao L, Niu Y, et al. (2017) 2-Substituted-thio-N-(4-substituted-thiazol/1H-imidazol-2-yl)acetamides as BACE1 inhibitors: Synthesis, biological evaluation and docking studies. European Journal of Medicinal Chemistry. 137: 462-475 |
| Zhou T, Cai Y, Liang L, et al. (2016) Discovery of a potent and highly specific β2 proteasome inhibitor from a library of copper complexes. Bioorganic & Medicinal Chemistry Letters |
| Yang L, Zhu Y, Shui M, et al. (2016) Rational Design of Fluorescent Phthalazinone Derivatives for One- and Two-Photon Imaging. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Yang L, Wang W, Sun Q, et al. (2016) Development of novel proteasome inhibitors based on phthalazinone scaffold. Bioorganic & Medicinal Chemistry Letters |
| Sun Q, Xu B, Niu Y, et al. (2015) Synthesis, bioactivity, docking and molecular dynamics studies of furan-based peptides as 20S proteasome inhibitors. Chemmedchem. 10: 498-510 |
| Liu P, Niu Y, Wang C, et al. (2014) 4-Oxo-1,4-dihydro-quinoline-3-carboxamides as BACE-1 inhibitors: synthesis, biological evaluation and docking studies. European Journal of Medicinal Chemistry. 79: 413-21 |
| Liang L, Wang W, Wu J, et al. (2013) Rational design, green synthesis, and initial evaluation of a series of full-color tunable fluorescent dyes enabled by the copper-catalyzed N-arylation of 6-phenyl pyridazinones and their application in cell imaging. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13774-82 |
| Liang L, Wang W, Xu F, et al. (2013) Relay catalysis by a multifunctional Cu catalyst in a tandem dehydro-/dehalogenation sequence along with N-arylation. Organic Letters. 15: 2770-3 |
| Cai YB, Liang L, Zhang J, et al. (2013) μ-Hydroxyl trinuclear copper(II) clusters: reactivity and unusual formation in the three-component synthesis of 1,2,3-triazoles in aqueous media. Dalton Transactions (Cambridge, England : 2003). 42: 5390-400 |
| Wang C, Xu F, Niu Y, et al. (2013) Synthesis and Biological Evaluations of 3-Benzothiazol-2-yl Coumarin Derivatives as MEK1 Inhibitors Letters in Drug Design & Discovery. 10: 727-732 |