Bing Zhou
Medical School
University of Chinese Academy of Sciences
Shanghai
Language: Chinese, English
Contact
Epigenetics Drug Discovery Innovative Drugs Histone Modification Gene Regulation Cancer Therapy Biomarkers Pharmacology Molecular Biology Clinical Trials Medicinal Chemistry Drug Design Synthesis Pharmacokinetics Pharmacodynamics Bioorganic Chemistry Chemical Biology Structure-Activity Relationship Lead Optimization Drug Metabolism C-H Activation Catalysis Organic Synthesis Reaction Mechanisms Transition Metals Functionalization Method Development Green Chemistry Synthetic Methods Chemical Reactions
Areas of Focus
  • Epigenetic Innovative Drug Research
  • Medicinal Chemistry
  • C-H Activation Methodology
Work Experience
  • 2016-03 to Present - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Researcher
  • 2013-04 to 2016-03 - University of Michigan, USA - Postdoctoral Researcher
  • 2011-06 to 2013-03 - Purdue University, USA - Postdoctoral Researcher
  • 2007-04 to 2008-08 - Hutchison MediPharma (Shanghai) Ltd. - Associate Researcher
Academic Background & Achievements
  • 2008-09 to 2011-06 PhD: Shanghai Institute of Materia Medica, Chinese Academy of Sciences
  • 2004-09 to 2007-03 Master's: Tongji University
  • 2000-09 to 2004-07 Bachelor's: Tongji University
Publications
  • Cyclization strategy leads to highly potent Bromodomain and extra-terminal (BET) Bromodomain inhibitors for the treatment of acute liver injury, Bing Zhou, 2023
  • Discovery of Highly Potent and Selective Thyroid Hormone Receptor Agonists for the Treatment of Nonalcoholic Steatohepatitis, Bing Zhou, 2023
  • Discovery of a Potent and Selective Degrader for USP7, Bing Zhou, 2022
  • The p300 Inhibitor A-485 Exerts Antitumor Activity in Growth Hormone Pituitary Adenoma, Bing Zhou, 2022
  • Rh(III)-catalyzed twofold unsymmetrical C-H alkenylation-annulation/amidation reaction enabled delivery of diverse furoquinazolinones, Bing Zhou, 2022
  • Discovery of novel Thieno2,3-dimidazole derivatives as agonists of human STING for antitumor immunotherapy using systemic administration, Bing Zhou, 2022
  • Celastrol recruits UBE3A to recognize and degrade the DNA binding domain of steroid receptors, Bing Zhou, 2022
  • Computational and Structure-Based Development of High Potent Cell-Active Covalent Inhibitor Targeting the Peptidyl-Prolyl Isomerase NIMA-Interacting-1 (Pin1), Bing Zhou, 2022
  • Potent and Selective RIPK1 Inhibitors Targeting Dual-Pockets for the Treatment of Systemic Inflammatory Response Syndrome and Sepsis, Bing Zhou, 2022
  • A potent PGK1 antagonist reveals PGK1 regulates the production of IL-1 and IL-6, Bing Zhou, 2022
  • Rhodium(III)-Catalyzed Asymmetric 1,2-Carboamidation of Alkenes Enables Access to Chiral 2,3-Dihydro-3-benzofuranmethanamides, Bing Zhou, 2022
  • The p300 Inhibitor A-485 Exerts Antitumor Activity in Growth Hormone Pituitary Adenoma, Bing Zhou, 2022
  • Design, synthesis and biological evaluation of a novel spiro oxazolidinedione as potent p300/CBP HAT inhibitor for the treatment of ovarian cancer, Bing Zhou, 2021
  • Discovery of a subtype-selective, covalent inhibitor against palmitoylation pocket of TEAD3, Bing Zhou, 2021
  • Rhodium-Catalyzed Twofold Unsymmetrical C-H Alkenylation-Annulation/Thiolation Reaction To Access Thiobenzofurans, Bing Zhou, 2021
  • P300/CBP inhibition sensitizes mantle cell lymphoma to PI3K delta inhibitor idelalisib, Bing Zhou, 2021
  • Rh(III)-catalyzed selective C7-H functionalization of indolines with 1,3-enynes enables access to six-membered 1,7-fused indolines, Bing Zhou, 2021
  • Discovery of thalidomide-based PROTAC small molecules as the highly efficient SHP2 degraders, Bing Zhou, 2021
  • Inhibition of autophagy by a small molecule through covalent modification of LC3 Protein, Bing Zhou, 2021
  • Design, synthesis, and biological evaluation of 4-benzoylamino-1H-pyrazole-3-carboxamide derivatives as potent CDK2 inhibitors, Bing Zhou, 2021
  • Rh(III)-catalyzed tandem annulative redox-neutral arylation/amidation of aromatic tethered alkenes, Bing Zhou, 2020
  • Design, synthesis, and biological evaluation of tetrahydroquinolin derivatives as potent inhibitors of CBP bromodomain, Bing Zhou, 2020
  • Ruthenium(II)-Catalyzed Regioselective C-H Hydroxymethylation of N-Aryl-azaindoles with Paraformaldehyde, Bing Zhou, 2020
  • Ruthenium(II)-Catalyzed Regioselective Ortho C-H Allenylation of Electron-Rich Aniline and Phenol Derivatives, Bing Zhou, 2020
  • Covalent Inhibitors Allosterically Block the Activation of Rho Family Proteins and Suppress Cancer Cell Invasion, Bing Zhou, 2020
  • Structure-based drug optimization and biological evaluation of tetrahydroquinolin derivatives as selective and potent CBP bromodomain inhibitors, Bing Zhou, 2020
  • BRD4 as a therapeutic target for nonfunctioning and growth hormone pituitary adenoma, Bing Zhou, 2020
  • Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors, Bing Zhou, 2020
  • Discovery of 8-Methyl-pyrrolo[1,2-a]pyrazin-1(2H)-one Derivatives as Highly Potent and Selective Bromodomain and Extra-terminal (BET) Bromodomain Inhibitors, Bing Zhou, 2020
  • Reduced asymmetric dimethylarginine accumulation through inhibition of the type I protein arginine methyltransferases promotes renal fibrosis in obstructed kidneys, Bing Zhou, 2019
  • p300/CBP inhibitor A-485 alleviates acute liver injury by regulating macrophage activation and polarization, Bing Zhou, 2019
  • Ru(II)-catalyzed regioselective C-7 hydroxymethylation of indolines with formaldehyde, Bing Zhou, 2019
  • Discovery and biological evaluation of vinylsulfonamide derivatives as highly potent, covalent TEAD autopalmitoylation inhibitors, Bing Zhou, 2019
  • Rh(III)-catalyzed Redox-Neutral Unsymmetrical C-H Alkylation and Amidation Reactions of N-Phenoxyacetamides, Bing Zhou, 2018
  • Rh(III)-Catalyzed C-H Functionalization of Indoles with Diazo Compounds: Facile Synthesis of Structurally Diverse 2,3-Fused Indoles, Bing Zhou, 2018
  • Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain Inhibitor, Bing Zhou, 2018
  • Discovery of QCA570 as an Exceptionally Potent and Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of the Bromodomain and Extra-Terminal (BET) Proteins Capable of Inducing Complete and Durable Tumor Regression, Bing Zhou
Awards
  • Shandong Province 'Outstanding Youth' (2024): Provincial Level
  • Pudong New Area 'Mingzhu Elite Talent' (2023): Other
  • Shandong Province Taishan Scholar Young Expert (2023): Provincial Level
  • Shanghai Outstanding Young Academic Leader (2022): Provincial Level
  • Shanghai Youth Science and Technology Star (2017): Provincial Level
  • National High-Level Talent Introduction Youth Talent (2017): National Level
  • Shanghai Pharmaceutical Science and Technology Award, Second Prize (2012): Provincial Level
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