27 articles for T Zhu
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
26
Structure-based design and synthesis of imidazo[1,2-a]pyridine derivatives as novel and potent Nek2 inhibitors with in vitro and in vivo antitumor activities.

East China Normal University
20
Discovery of core-structurally novel PTP1B inhibitors with specific selectivity containing oxindole-fused spirotetrahydrofurochroman by one-pot reaction.

East China Normal University
77
Tyrosine Kinase Inhibitors. 20. Optimization of Substituted Quinazoline and Pyrido[3,4-d]pyrimidine Derivatives as Orally Active, Irreversible Inhibitors of the Epidermal Growth Factor Receptor Family.

University of Auckland
43
Pharmacophore identification of Raf-1 kinase inhibitors.

China Pharmaceutical University
4
Isolation and structure of homotemsirolimuses A, B, and C.

Wyeth Research
7
Discovery of a clinical candidate from the structurally unique dioxa-bicyclo[3.2.1]octane class of sodium-dependent glucose cotransporter 2 inhibitors.

Pfizer
23
C-Aryl glycoside inhibitors of SGLT2: Exploration of sugar modifications including C-5 spirocyclization.

Pfizer
51
Virtual screening for Raf-1 kinase inhibitors based on pharmacophore model of substituted ureas.

China Pharmaceutical University
28
Discovery of Chalcone Derivatives as Bifunctional Molecules with Anti-SARS-CoV-2 and Anti-inflammatory Activities.

East China Normal University
3
Design, synthesis, and biological evaluation of novel penindolone derivatives as potential inhibitors of hemagglutinin-mediated membrane fusion.

Ocean University of China
8
Antibacterial oxazolidinones possessing a novel C-5 side chain. (5R)-trans-3-[3-Fluoro-4- (1-oxotetrahydrothiopyran-4-yl)phenyl]-2- oxooxazolidine-5-carboxylic acid amide (PF-00422602), a new lead compound.

Pfizer
30
Function-oriented synthesis of Imidazo[1,2-a]pyrazine and Imidazo[1,2-b]pyridazine derivatives as potent PI3K/mTOR dual inhibitors.

East China Normal University
24
The synthesis and biological evaluation of novel series of nitrile-containing fluoroquinolones as antibacterial agents.

Pfizer
13
CLIPSing Melanotan-II to Discover Multiple Functionally Selective hMCR Agonists.

University of Naples Federico II
15
Design and synthesis of 5-aryl-pyridone-carboxamides as inhibitors of anaplastic lymphoma kinase.

Chembridge Research Laboratories and Chembridge
2
Discovery of novel coumarin-indole derivatives as tubulin polymerization inhibitors with potent anti-gastric cancer activities.

Zhengzhou University
1
Novel tertiary sulfonamide derivatives containing benzimidazole moiety as potent anti-gastric cancer agents: Design, synthesis and SAR studies.

Zhengzhou University
3
Chemoreactive-Inspired Discovery of Influenza A Virus Dual Inhibitor to Block Hemagglutinin-Mediated Adsorption and Membrane Fusion.

Ocean University of China
19
Design, Synthesis, and Biological Evaluation of Imidazo[1,2-

East China Normal University
1
Discovery of 1,2,4-triazine-based derivatives as novel neddylation inhibitors and anticancer activity studies against gastric cancer MGC-803 cells.

Zhengzhou University
2
Phenylspirodrimanes with anti-HIV activity from the sponge-derived fungus Stachybotrys chartarum MXH-X73.

Ocean University of China
2
Aspulvinones from a mangrove rhizosphere soil-derived fungus Aspergillus terreus Gwq-48 with anti-influenza A viral (H1N1) activity.

Ocean University of China
15
1-methyl-4-[(4-phenylphenyl)sulfonylmethyl]cyclohexyanol and 1-methyl-4-[[4-(2-pyridyl)phenyl]sulfonylmethyl]cyclohexanol compounds and their therapeutic use

Modern Biosciences
25
Indoleamine-2,3-dioxygenase inhibitor, preparation method therefor and use thereof

Hinova Pharmaceuticals
32
SHMT inhibitors

The Trustees of Princeton University
11
Antidiabetic bicyclic compounds

Merch Sharp & Dohne Corp. Rahway
24
Compounds and methods for skin repair

Allergan