Synthesis and biological evaluation of new [1,2,4]triazolo[4,3-a]pyridine derivatives as potential c-Met inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of new [1,2,4]triazolo[4,3-a]pyridine derivatives as potential c-Met inhibitors

Published:2016-08 Issue:16 Volume:24 Page:3483-3493
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Zhao Junjun,Fang Lei,Zhang Xiaobing,Liang Yan,Gou Shaohua

Funder

Jiangsu Province Hi-Tech Key Laboratory for Biomedical Research

Jiangsu Hansoh Pharmaceutical Corporation

Priority Academic Program Development of Jiangsu Higher Education Institutions

Natural Science Foundation of Jiangsu Province

Publisher

Elsevier BV

Subject

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

Reference28 articles.

1. Targeting c-Met as a promising strategy for the treatment of hepatocellular carcinoma

2. c-met tyrosine kinase receptor expression is associated with abnormal β-catenin expression and favourable prognostic factors in invasive breast carcinoma

3. Targeting the c-Met Signaling Pathway in Cancer: Fig. 1.

4. Targeting the HGF/c-Met Axis: State of Play

5. From Concept to Reality: The Long Road to c-Met and RON Receptor Tyrosine Kinase Inhibitors for the Treatment of Cancer

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1. Machine Learning, Molecular Docking, and Dynamics-Based Computational Identification of Potential Inhibitors against Lung Cancer;ACS Omega;2024-01-17

2. Design, Synthesis and Pharmacological Evaluation of Novel Thiazole-Based Peptide Like Molecules as C-Met Kinase Inhibitors and Anticancer Agents;2024

3. Fused Pyridine Derivatives: Synthesis and Biological Activities;Exploring Chemistry with Pyridine Derivatives;2023-01-04

4. Discovery of new PKN2 inhibitory chemotypes via QSAR-guided selection of docking-based pharmacophores;Molecular Diversity;2022-05-04

5. Synthesis and Thione–Thiol Tautomerism of 5-Thioxopyrano[3,4-c][1,2,4]triazolo[4,3-a]pyridines;Russian Journal of Organic Chemistry;2020-08

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