Pyridine-derived VEGFR-2 inhibitors: Rational design, synthesis, anticancer evaluations, in silico ADMET profile, and molecular docking.


Journal

Archiv der Pharmazie
ISSN: 1521-4184
Titre abrégé: Arch Pharm (Weinheim)
Pays: Germany
ID NLM: 0330167

Informations de publication

Date de publication:
Aug 2021
Historique:
revised: 02 04 2021
received: 03 03 2021
accepted: 06 04 2021
pubmed: 6 5 2021
medline: 31 12 2021
entrez: 5 5 2021
Statut: ppublish

Résumé

Novel pyridine-derived compounds (5-19) were designed and synthesized, and their anticancer activities were evaluated against HepG2 and MCF-7 cells, targeting the VEGFR-2 enzyme. Compounds 10, 9, 8, and 15 were found to be the most potent derivatives against the two cancer cell lines, HepG2 and MCF-7, respectively, with IC

Identifiants

pubmed: 33948983
doi: 10.1002/ardp.202100085
doi:

Substances chimiques

Antineoplastic Agents 0
Pyridines 0
Doxorubicin 80168379AG
Sorafenib 9ZOQ3TZI87
KDR protein, human EC 2.7.10.1
Vascular Endothelial Growth Factor Receptor-2 EC 2.7.10.1

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2100085

Informations de copyright

© 2021 Deutsche Pharmazeutische Gesellschaft.

Références

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Auteurs

Nashwa M Saleh (NM)

Department of Chemistry, Faculty of Science, Al-Azhar University (Girls Branch), Cairo, Egypt.

Adel A-H Abdel-Rahman (AA)

Department of Chemistry, Faculty of Science, Menoufia University, Shebin El-Koam, Egypt.

Asmaa M Omar (AM)

Department of Chemistry, Faculty of Science, Menoufia University, Shebin El-Koam, Egypt.

Mohamed M Khalifa (MM)

Department of Pharmaceutical Medicinal Chemistry and Drug Design, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo, Egypt.

Khaled El-Adl (K)

Department of Pharmaceutical Medicinal Chemistry and Drug Design, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo, Egypt.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Heliopolis University for Sustainable Development, Cairo, Egypt.

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