Gary T. Wang
Abbott Fund(US)
Publications by Year
Research Areas
Click Chemistry and Applications, Peptidase Inhibition and Analysis, Alzheimer's disease research and treatments, Chemical Synthesis and Analysis, HIV/AIDS drug development and treatment
Most-Cited Works
- → Novel Fluorogenic Substrates for Assaying Retroviral Proteases by Resonance Energy Transfer(1990)593 cited
- → Design, Synthesis, and Structural Analysis of Influenza Neuraminidase Inhibitors Containing Pyrrolidine Cores(2001)132 cited
- → Synthetic chemical diversity: solid phase synthesis of libraries of C2 symmetric inhibitors of HIV protease containing diamino diol and diamino alcohol cores(1995)78 cited
- → Involvement of Cell Surface Glycosyl-phosphatidylinositol-linked Aspartyl Proteases in α-Secretase-type Cleavage and Ectodomain Solubilization of Human Alzheimer β-Amyloid Precursor Protein in Yeast(1998)66 cited
- → Design and synthesis of new fluorogenic HIV protease substrates based on resonance energy transfer(1990)64 cited
- → Discovery and Optimization of Anthranilic Acid Sulfonamides as Inhibitors of Methionine Aminopeptidase-2: A Structural Basis for the Reduction of Albumin Binding(2006)60 cited
- → Imidazo[2,1-b]thiazoles: Multitargeted inhibitors of both the insulin-like growth factor receptor and members of the epidermal growth factor family of receptor tyrosine kinases(2010)56 cited
- → Purification and Characterization of the Yeast Glycosylphosphatidylinositol-anchored, Monobasic-specific Aspartyl Protease Yapsin 2 (Mkc7p)(1999)52 cited
- → Internally Consistent Libraries of Fluorogenic Substrates Demonstrate That Kex2 Protease Specificity Is Generated by Multiple Mechanisms(1997)49 cited
- → 1-(5-Chloro-2-alkoxyphenyl)-3-(5-cyano- pyrazi-2-yl)ureas as Potent and Selective Inhibitors of Chk1 Kinase: Synthesis, Preliminary SAR, and Biological Activities(2005)42 cited