Design, synthesis, docking, ADMET profile, and anticancer evaluations of novel thiazolidine-2,4-dione derivatives as VEGFR-2 inhibitors.
Antineoplastic Agents
/ chemical synthesis
Dose-Response Relationship, Drug
Drug Design
HCT116 Cells
Hep G2 Cells
Humans
Inhibitory Concentration 50
MCF-7 Cells
Molecular Docking Simulation
Neoplasms
/ drug therapy
Protein Kinase Inhibitors
/ chemical synthesis
Sorafenib
/ pharmacology
Structure-Activity Relationship
Thiazolidinediones
/ chemical synthesis
Vascular Endothelial Growth Factor Receptor-2
/ antagonists & inhibitors
HCT-116
HepG2
MCF-7
VEGFR-2 inhibitors
anticancer agents
molecular docking
thiazolidine-2,4-dione
Journal
Archiv der Pharmazie
ISSN: 1521-4184
Titre abrégé: Arch Pharm (Weinheim)
Pays: Germany
ID NLM: 0330167
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
revised:
23
02
2021
received:
28
12
2020
accepted:
26
02
2021
pubmed:
1
4
2021
medline:
15
12
2021
entrez:
31
3
2021
Statut:
ppublish
Résumé
The anticancer activity of novel thiazolidine-2,4-diones was evaluated against HepG2, HCT-116, and MCF-7 cells. Among the tested cancer cell lines, HCT-116 was the most sensitive one to the cytotoxic effect of the new derivatives. In particular, compounds 18, 11, and 10 were found to be the most potent derivatives among all the tested compounds against the HepG2, HCT-116, and MCF-7 cancer cell lines, with IC
Identifiants
pubmed: 33788290
doi: 10.1002/ardp.202000491
doi:
Substances chimiques
Antineoplastic Agents
0
Protein Kinase Inhibitors
0
Thiazolidinediones
0
thiazolidine-2,4-dione
0
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
e2000491Informations de copyright
© 2021 Deutsche Pharmazeutische Gesellschaft.
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