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Publications by Changjin Zhu
Novel 2-Phenoxypyrido[3,2-B]pyrazin-3(4h)-One Derivatives as Potent and Selective Aldose Reductase Inhibitors With Antioxidant Activity
Journal of Enzyme Inhibition and Medicinal Chemistry
Medicine
Drug Discovery
Pharmacology
2-[1,1-Dioxo-2-(2,4,5-Trifluorobenzyl)-2h-1,2-Benzothiazin-4-Yl]acetic Acid
Acta Crystallographica Section E Structure Reports Online
Related publications
Synthesis and Biological Evaluation of New Piplartine Analogues as Potent Aldose Reductase Inhibitors (ARIs)
European Journal of Medicinal Chemistry
Medicine
Organic Chemistry
Drug Discovery
Pharmacology
Furan-2-Ylmethylene Thiazolidinediones as Novel, Potent, and Selective Inhibitors of Phosphoinositide 3-Kinase G
Matteuorienate a and B, Two New and Potent Aldose Reductase Inhibitors From Matteuccia Orientalis (HOOK.)TREV.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Preparations of 5-Alkylmethylidene-3-Carboxymethylrhodanine Derivatives and Their Aldose Reductase Inhibitory Activity.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Studies on Antidiabetic Agents. III. 5-Arylthiazolidine-2,4-Diones as Potent Aldose Reductase Inhibitors.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Ligand-Based Drug Design of Novel Aldose Reductase Inhibitors
Future Medicinal Chemistry
Drug Discovery
Molecular Medicine
Pharmacology
Aldose Reductase Inhibitors: 2013-Present
Expert Opinion on Therapeutic Patents
Medicine
Drug Discovery
Pharmacology
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
