Zhongqi Shen
Northeast Forestry University(CN)
Publications by Year
Research Areas
Biochemical and Molecular Research, Cytomegalovirus and herpesvirus research, Adenosine and Purinergic Signaling, HIV/AIDS drug development and treatment, Synthesis and Catalytic Reactions
Most-Cited Works
- → 2-Aminothiazole as a Novel Kinase Inhibitor Template. Structure−Activity Relationship Studies toward the Discovery of N -(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (Dasatinib, BMS-354825) as a Potent pan -Src Kinase Inhibitor(2006)395 cited
- → A new facile method for the synthesis of 1-arylimidazole-5-carboxylates(2000)178 cited
- → Molecular design, synthesis, and structure–Activity relationships leading to the potent and selective p56lck inhibitor BMS-243117(2003)58 cited
- → Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56Lck(2003)57 cited
- → Acridone-Based Inhibitors of Inosine 5‘-Monophosphate Dehydrogenase: Discovery and SAR Leading to the Identification of N-(2-(6-(4-Ethylpiperazin-1-yl)pyridin-3-yl)propan-2-yl)-2- fluoro-9-oxo-9,10-dihydroacridine-3-carboxamide (BMS-566419)(2007)49 cited
- → Total Synthesis of d,l-Isospongiadiol: An Intramolecular Radical Cascade Approach to Furanoditerpenes(1996)43 cited
- → Discovery of N-[2-[2-[[3-Methoxy-4-(5-oxazolyl)phenyl]amino]-5-oxazolyl]phenyl]-N-methyl-4- morpholineacetamide as a Novel and Potent Inhibitor of Inosine Monophosphate Dehydrogenase with Excellent in Vivo Activity(2002)41 cited
- → Rapid synthesis of triazine inhibitors of inosine monophosphate dehydrogenase(2002)40 cited
- → Novel indole-based inhibitors of IMPDH: introduction of hydrogen bond acceptors at indole C-3(2003)39 cited
- → Discovery and initial SAR of imidazoquinoxalines as inhibitors of the Src-family kinase p56Lck(2002)37 cited