Bin Guo
guobin@simm.ac.cn
Chinese, English
Shanghai
University of Chinese Academy of Sciences
Medical School
  • 2007-09--2012-06 PhD: Shanghai Institute of Materia Medica, Chinese Academy of Sciences
  • 2003-09--2007-06 Bachelor's Degree: Wuhan University
  • 2021-10~Present - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Researcher
  • 2014-10~2021-09 - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Associate Researcher
  • 2012-07~2014-09 - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Assistant Researcher
  • 2024-01-01~Present - Nanjing University of Chinese Medicine - Master's Supervisor
Anti-infection drug development
Antitumor drug development
Antithrombotic drug development
  • Efficient Kilogram-Scale Synthesis of a Novel Oxazolidinone Antibacterial Candidate YG-056SP, 5th Author, 2023
  • Improved Synthesis of Key Intermediate of Baloxavir Marboxil, an Anti-Influenza Drug, 4th Author, 2022
  • Discovery of Thieno2,3-eindazole Derivatives as Novel Oral Selective Estrogen Receptor Degraders with Highly Improved Antitumor Effect and Favorable Druggability, 5th Author, 2022
  • Design, Synthesis, and Biological Evaluation of Novel Pyrimido4,5-bindole Derivatives Against Gram-Negative Multidrug-Resistant Pathogens, 5th Author, 2021
  • Improved Practical Synthesis of DY-038, an Oral Available Antiplatelet Agent, 6th Author, 2021
  • Improved synthesis of YG-056SP, a potent oxazolidinone antibacterial candidate against multi-drug resistant bacteria, 7th Author, 2019
  • Optimization of P2Y12 Antagonist Ethyl 6-(4-((Benzylsulfonyl)carbamoyl)piperidin-1-yl)-5-cyano-2-methylnicotinate (AZD1283) Led to the Discovery of an Oral Antiplatelet Agent with Improved Druglike Properties, 1st Author, 2019
  • Design, Synthesis, and Biological Evaluation of Novel DNA Gyrase-Inhibiting Spiropyrimidinetriones as Potent Antibiotics for Treatment of Infections Caused by Multidrug-Resistant Gram-Positive Bacteria, 6th Author, 2019
  • Synthesis and biological evaluation of novel potent FFA1 agonists containing 2,3-dihydrobenzob1,4dioxine, 4th Author, 2019
  • Design and optimization of 2,3-dihydrobenzob1,4dioxine propanoic acids as novel GPR40 agonists with improved pharmacokinetic and safety profiles, 1st Author, 2018
  • Design, synthesis and evaluation of potent G-protein coupled receptor 40 agonists, 2nd Author, 2016
  • Synthesis and structure-activity relationship studies of novel 6,6,5 tricyclic oxazolidinone derivatives as potential antibacterial agents, 3rd Author, 2015
  • Design, Synthesis, and Structure-Activity and Structure-Pharmacokinetic Relationship Studies of Novel 6,6,5 Tricyclic Fused Oxazolidinones Leading to the Discovery of a Potent, Selective, and Orally Bioavailable FXa Inhibitor, 3rd Author, 2014
  • Synthesis and biological evaluation of novel benzoxazinyl-oxazolidinones as potential antibacterial agents, 1st Author, 2013
  • Solubility-Driven Optimization of (Pyridin-3-yl) Benzoxazinyl-oxazolidinones Leading to a Promising Antibacterial Agent, 1st Author, 2013
  • Design, Synthesis, and Structure-Activity Relationship Studies of Highly Potent Novel Benzoxazinyl-Oxazolidinone Antibacterial Agents, 3rd Author, 2011
Anti-Infection Antitumor Antithrombotic Drug Development Small Molecules Innovative Drugs Research Pharmaceuticals Medicinal Chemistry Clinical Research

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