Xiangrui Jiang
jiangxiangrui@simm.ac.cn
Chinese, English
Shanghai
University of Chinese Academy of Sciences
Medical School
  • 2002-09--2005-12 PhD: Zhejiang University
  • 1999-09--2002-06 Master's: Central China Normal University
  • 1995-09--1999-06 Bachelor's: Wuhan Institute of Technology
  • 2008-07~Present - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Assistant Researcher, Associate Researcher, Researcher, Group Leader
  • 2006-03~2008-06 - Shanghai Institute of Materia Medica, Chinese Academy of Sciences - Postdoctoral Researcher
  • 2002-09~2005-12 - Zhejiang University - PhD
  • 1999-09~2002-06 - Central China Normal University - Master's
  • 1995-09~1999-06 - Wuhan Institute of Technology - Bachelor's
  • Outstanding Communist Party Member of Shanghai Branch, Chinese Academy of Sciences (2022): Other
  • May Fourth Youth Commando of Shanghai Branch, Chinese Academy of Sciences (2021): Municipal Level
  • Commemorative Medal for Fighting COVID-19, Shanghai Institute of Materia Medica (2020): Institute Level
Small Molecule Structure-Activity Relationship Research
Modification of Natural Product Structures
Drug Synthesis Process Research
  • Preventive and therapeutic benefits of nelfinavir in rhesus macaques and human beings infected with SARS-CoV-2, 5th Author, 2023
  • Structure-based development and preclinical evaluation of the SARS-CoV-2 3C-like protease inhibitor simnotrelvir, 1st Author, 2023
  • Design, synthesis and biological evaluation of peptidomimetic benzothiazolyl ketones as 3CL pro inhibitors against SARS-CoV-2, 8th Author, 2023
  • Design, synthesis and biological evaluation of covalent peptidomimetic 3CL protease inhibitors containing nitrile moiety, 9th Author, 2023
  • Synthesis, cytotoxicity, and pharmacokinetic evaluations of niclosamide analogs for anti-SARS-CoV-2, 8th Author, 2023
  • Synthesis and biological evaluation of artemisinin derivatives as potential MS agents, 11th Author, 2022
  • Molecular recognition of morphine and fentanyl by the human μ-opioid receptor, 14th Author, 2022
  • Artemisinin derivative TPN10466 suppresses immune cell migration and Th1/Th17 differentiation to ameliorate disease severity in experimental autoimmune encephalomyelitis, 2nd Author, 2022
  • 9,10-Anhydrodehydroartemisinin Attenuates Experimental Autoimmune Encephalomyelitis by Inhibiting Th1 and Th17 Cell Differentiation, 11th Author, 2021
  • SARS-CoV-2 envelope protein causes acute respiratory distress syndrome (ARDS)-like pathological damages and constitutes an antiviral target, 13th Author, 2021
  • Identification of pyrogallol as a warhead in design of covalent inhibitors for the SARS-CoV-2 3CL protease, 13th Author, 2021
  • Improved Synthesis of 6-Chloro-5-methylpyridin-2-amine: A Key Intermediate for Making Lumacaftor, 11th Author, 2020
  • The novel small-molecule TPN10456 inhibits Th17 cell differentiation and protects against experimental autoimmune encephalomyelitis, 3rd Author, 2020
  • Targeted Drugs for Treatment of Pulmonary Arterial Hypertension: Past, Present, and Future Perspectives, 3rd Author, 2020
  • Automated design and optimization of multitarget schizophrenia drug candidates by deep learning, 2nd Author, 2020
  • Oxidative Aromatization of 3,4-Dihydroquinolin-2(1H)-ones to Quinolin-2(1H)-ones Using Transition-Metal-Activated Persulfate Salts, 6th Author, 2019
  • Metal-free quinolylation of the primary amino groups of amino acid derivatives and peptides with dihydrooxazolo3,2-aquinoliniums, 10th Author, 2019
  • Nature brings new avenues to the therapy of central nervous system diseases--an overview of possible treatments derived from natural products, 3rd Author, 2019
  • Pharmacokinetics-driven optimization of 4(3h)-pyrimidinones as phosphodiesterase type 5 inhibitors leading to tpn171, a clinical candidate for the treatment of pulmonary arterial hypertension, 2nd Author, 2019
  • Rational design of 5-((1H-imidazol-1-yl)methyl)quinolin-8-ol derivatives as novel bromodomain-containing protein 4 inhibitors, 3rd Author, 2019
  • Continuation of structure-activity relationship study of novel benzamide derivatives as potential antipsychotics, 6th Author, 2019
  • Characterization of TPN171 metabolism in humans via ultra-performance liquid chromatography/quadrupole time-of-flight Checir for mass spectrometry, 4th Author, 2019
  • Discovery of pyrimidine nucleoside dual prodrugs and pyrazine nucleosides as novel anti-HCV agents, 5th Author, 2019
  • Synthesis and biological evaluation of a series of novel pyridinecarboxamides as potential multi-receptor antipsychotic drugs, 7th Author, 2018
  • Synthesis and biological evaluation of a series of multi-target N-substituted cyclic imide derivatives with potential antipsychotic effect, 7th Author, 2018
  • Synthesis and biological investigation of tetrahydropyridopyrimidinone derivatives as potential multireceptor atypical antipsychotics, 7th Author, 2017
  • Synthesis of Impurities of Pramipexole Dihydrochloride, 11th Author, 2016
  • Research progress of antipsychotics, 5th Author, 2016
  • Synthesis, structure-activity relationships, and biological evaluation of a series of benzamides as potential multireceptor antipsychotics, 2nd Author, 2016
  • Nucleoside Inhibitors of Hepatitis C Virus NS5B Polymerase: A Systematic Review, 3rd Author, 2016
  • Improved Synthesis of 4-(1-Piperazinyl)benzo[b]thiophene Dihydrochloride, 11th Author, 2015
  • Design, Synthesis, and Pharmacological Evaluation of Highly Potent and Selective Dipeptidyl Peptidase-4 Inhibitors, 11th Author, 2015
  • A neighboring group participation strategy: facile synthesis of 3,5-di-O-benzoyl-2-C-methyl-D-arabino-gamma-lactone, 6th Author, 2015
  • Design, Synthesis, and Pharmacological Evaluationof Fused β-Homophenylalanine Derivatives as Potent DPP-4Inhibitors, 9th Author, 2015
  • New Synthesis of N-(4-Chloro-3-cyano-7-ethoxyquinolin-6-yl)acetamide, 11th Author, 2015
  • Design, Synthesis, and Pharmacological Evaluation of Fused beta-Homophenylalanine Derivatives as Potent DPP-4 Inhibitors, 11th Author, 2015
  • An Improved Synthesis of 4-(1-Piperazinyl)benzobthiophene Dihydrochloride, 11th Author, 2015
  • Improvement of the Process for Sodium Gslycocholate, 3rd Author, 2014
  • Tapentadol enantiomers: Synthesis, physico-chemical characterization and cyclodextrin interactions, 9th Author, 2014
  • Astemizole arrests the proliferation of cancer cells by disrupting the EZH2-EED interaction of polycomb repressive complex 2., 4th Author, 2014
  • The Selectivity and Potency of the New PDE5 Inhibitor TPN729MA, 5th Author, 2013
  • Exploration of the 5-bromopyrimidin-4(3H)-ones as potent inhibitors of PDE5., 8th Author, 2013
  • A New and Improved Process for N-(4-Chloro-3-cyano-7-ethoxyquinolin-6-yl)acetamide, 7th Author, 2012
  • A practical and enantioselective synthesis of tapentadol, 11th Author, 2012
  • Synthesis of Telmisartan, 2nd Author, 2012
  • Design, synthesis, and pharmacological evaluation of monocyclic pyrimidinones as novel inhibitors of PDE5.
Small Molecule Structure-Activity Relationship Natural Products Modification Drug Synthesis Process Research Pharmaceutical Chemistry Bioorganic Chemistry Medicinal Chemistry Synthetic Methods

Contact us

Let's talk!
* Required
* Required
* Required
* Invalid email address
By submitting this form, you agree that IoT ONE may contact you with insights and marketing messaging.
No thanks, I don't want to receive any marketing emails from IoT ONE.
Submit

Thank you for your message!
We will contact you soon.