Design, synthesis, and docking of novel thiazolidine-2,4-dione multitarget scaffold as new approach for cancer treatment.
Humans
Structure-Activity Relationship
Cell Line, Tumor
Thiazolidines
/ pharmacology
Vascular Endothelial Growth Factor Receptor-2
/ metabolism
ErbB Receptors
/ metabolism
Antineoplastic Agents
Protein Kinase Inhibitors
/ pharmacology
Molecular Docking Simulation
Lung Neoplasms
Mutation
Drug Screening Assays, Antitumor
Cell Proliferation
Molecular Structure
4-dione
anticancer agents
dual inhibitors of VEGFR-2/EGFRT790M
molecular docking
thiazolidine-2
Journal
Archiv der Pharmazie
ISSN: 1521-4184
Titre abrégé: Arch Pharm (Weinheim)
Pays: Germany
ID NLM: 0330167
Informations de publication
Date de publication:
Jul 2023
Jul 2023
Historique:
revised:
17
04
2023
received:
07
03
2023
accepted:
18
04
2023
medline:
6
7
2023
pubmed:
6
5
2023
entrez:
6
5
2023
Statut:
ppublish
Résumé
Novel thiazolidine-2,4-diones have been developed and estimated as conjoint inhibitors of EGFR
Identifiants
pubmed: 37147779
doi: 10.1002/ardp.202300137
doi:
Substances chimiques
Thiazolidines
0
Vascular Endothelial Growth Factor Receptor-2
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Antineoplastic Agents
0
thiazolidine-2,4-dione
0
Protein Kinase Inhibitors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2300137Subventions
Organisme : Princess Nourah bint Abdulrahman University
Informations de copyright
© 2023 Deutsche Pharmazeutische Gesellschaft.
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