Guo Zhu Zheng
Institute for Biomedicine(IT)
Publications by Year
Research Areas
Chemical Synthesis and Analysis, Pain Mechanisms and Treatments, Quinazolinone synthesis and applications, Synthesis and Reactivity of Heterocycles, Synthesis and biological activity
Most-Cited Works
- → Novel Transient Receptor Potential Vanilloid 1 Receptor Antagonists for the Treatment of Pain: Structure−Activity Relationships for Ureas with Quinoline, Isoquinoline, Quinazoline, Phthalazine, Quinoxaline, and Cinnoline Moieties(2005)163 cited
- → Regiocontrolled Hydrosilation of .alpha.,.beta.-Unsaturated Carbonyl Compounds Catalyzed by Hydridotetrakis(triphenylphosphine)rhodium(I)(1995)125 cited
- → Catalytic reactions of samarium (II) iodide(1997)114 cited
- → Discovery of Selective Estrogen Receptor Covalent Antagonists for the Treatment of ERαWT and ERαMUT Breast Cancer(2018)109 cited
- → Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets(2007)99 cited
- → Structure−Activity Relationship of Triazafluorenone Derivatives as Potent and Selective mGluR1 Antagonists(2005)71 cited
- → Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A‐841720, a novel non‐competitive mGluR1 receptor antagonist(2006)50 cited
- → Tetrahydropyridine-4-carboxamides as novel, potent transient receptor potential vanilloid 1 (TRPV1) antagonists(2008)48 cited
- → 5-(3-Bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-ylamine: structure–activity relationships of 7-substituted heteroaryl analogs as non-nucleoside adenosine kinase inhibitors(2005)48 cited
- → Adenosine kinase inhibitors: polar 7-Substitutent of pyridopyrimidine derivatives improving their locomotor selectivity(2003)43 cited