Biochemical characterization of a novel type-II VEGFR2 kinase inhibitor: Comparison of binding to non-phosphorylated and phosphorylated VEGFR2-Reference-Cited by-同舟云学术

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Biochemical characterization of a novel type-II VEGFR2 kinase inhibitor: Comparison of binding to non-phosphorylated and phosphorylated VEGFR2

Published:2011-09 Issue:18 Volume:19 Page:5342-5351
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Iwata Hidehisa,Imamura Shinichi,Hori Akira,Hixon Mark S.,Kimura Hiroyuki,Miki Hiroshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference34 articles.

1. The Protein Kinase Complement of the Human Genome

2. Protein Tyrosine Kinase Structure and Function

3. Oncogenic kinase signalling

4. Autoregulatory Mechanisms in Protein-tyrosine Kinases

5. Strategies toward the Design of Novel and Selective Protein Tyrosine Kinase Inhibitors

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1. Synthesis and Characterization of Reversible Covalent HDAC4 Inhibitors;Methods in Molecular Biology;2022-10-19

2. Classical MD and metadynamics simulations on back-pocket binders of CDK2 and VEGFR2: a guidepost to design novel small-molecule dual inhibitors;Journal of Biomolecular Structure and Dynamics;2021-05-05

3. Kinetics of Drug Binding and Residence Time;Annual Review of Physical Chemistry;2019-06-14

4. Exploration for novel inhibitors showing back-to-front approach against VEGFR-2 kinase domain (4AG8) employing molecular docking mechanism and molecular dynamics simulations;BMC Cancer;2018-03-07

5. Anticancer Properties of Halogenated Pyrrolo[3,2-d ]pyrimidines with Decreased Toxicity via N5 Substitution;ChemMedChem;2017-12-18

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