Design, Synthesis, and Molecular Docking Studies of 5‐Bromoindole‐2‐Carboxylic Acid Hydrazone Derivatives: In Vitro Anticancer and VEGFR‐2 Inhibitory Effects-Reference-Cited by-同舟云学术

Design, Synthesis, and Molecular Docking Studies of 5‐Bromoindole‐2‐Carboxylic Acid Hydrazone Derivatives: In Vitro Anticancer and VEGFR‐2 Inhibitory Effects

Published:2022-12-08 Issue:46 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Hassan Omeed M.¹,Razzak Mahmood Ammar A.²,Hamzah Ali H.³,Tahtamouni Lubna H.⁴⁵^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, College of Pharmacy University of Kirkuk Kirkuk Iraq

2. Department of Pharmaceutical Chemistry, College of Pharmacy University of Baghdad Bagdad Iraq

3. Department of Medicinal and Biological Chemistry University of Toledo Toledo Ohio USA

4. Department of Biology and Biotechnology, Faculty of Science The Hashemite University Zarqa 13133 Jordan

5. Department of Biochemistry and Molecular Biology, College of Natural Sciences Colorado State University Fort Collins 80523 Colorado USA

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202203726

Reference31 articles.

1. Novel [1,2,3]triazolo[4,5-d]pyrimidine derivatives containing hydrazone fragment as potent and selective anticancer agents

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4. Inhibition of FGF‐FGFR and VEGF‐VEGFR signalling in cancer treatment

5. Mechanisms and regulation of endothelial VEGF receptor signalling

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