Quinazoline based 1,3,5‐triazine derivatives as cancer inhibitors by impeding the phosphorylated RET tyrosine kinase pathway: Design, synthesis, docking, and QSAR study-Reference-Cited by-同舟云学术

Quinazoline based 1,3,5‐triazine derivatives as cancer inhibitors by impeding the phosphorylated RET tyrosine kinase pathway: Design, synthesis, docking, and QSAR study

Published:2019-08-05 Issue:9 Volume:352 Page:1900053
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:en
Short-container-title:Arch Pharm Chem Life Sci

Author:

Pathak Prateek¹^ORCID,Naumovich Vladislav¹,Grishina Maria¹^ORCID,Shukla Parjanya Kumar²,Verma Amita²^ORCID,Potemkin Vladimir¹^ORCID

Affiliation:

1. Laboratory of Computational Modeling of Drugs, Higher Medical and Biological SchoolSouth Ural State University Chelyabinsk Russia

2. Sam Higginbottom University of Agriculture Technology and Sciences Allahabad Uttar Pradesh India

Funder

Russian Foundation for Basic Research

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ardp.201900053

Reference53 articles.

1. Design, synthesis and biological evaluation of quinoline amide derivatives as novel VEGFR-2 inhibitors

2. Anti-angiogenic therapy for cancer: current progress, unresolved questions and future directions

3. Design, synthesis and biological evaluation of new classes of thieno[3,2-d]pyrimidinone and thieno[1,2,3]triazine as inhibitor of vascular endothelial growth factor receptor-2 (VEGFR-2)

4. Synthesis of novel diarylamino-1,3,5-triazine derivatives as FAK inhibitors with anti-angiogenic activity

5. Discovery and molecular docking of quinolyl-thienyl chalcones as anti-angiogenic agents targeting VEGFR-2 tyrosine kinase

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