Potential of substituted quinazolines to interact with multiple targets in the treatment of cancer.
Antineoplastic Agents
/ chemical synthesis
Cell Line, Tumor
Cell Proliferation
/ drug effects
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
ErbB Receptors
/ antagonists & inhibitors
Humans
Molecular Structure
Protein Kinase Inhibitors
/ chemical synthesis
Quinazolines
/ chemical synthesis
Structure-Activity Relationship
Vascular Endothelial Growth Factor Receptor-2
/ antagonists & inhibitors
Angiogenesis
Microtubule targeting agents
Multi-target inhibitors
Quinazolines
Receptor tyrosine kinase
Journal
Bioorganic & medicinal chemistry
ISSN: 1464-3391
Titre abrégé: Bioorg Med Chem
Pays: England
ID NLM: 9413298
Informations de publication
Date de publication:
01 04 2021
01 04 2021
Historique:
received:
11
11
2020
revised:
28
01
2021
accepted:
01
02
2021
pubmed:
2
3
2021
medline:
16
9
2021
entrez:
1
3
2021
Statut:
ppublish
Résumé
The efficacy of quinazoline-based antiglioma agents has been attributed to their effects on microtubule dynamics.
Identifiants
pubmed: 33647840
pii: S0968-0896(21)00069-9
doi: 10.1016/j.bmc.2021.116061
pmc: PMC7995636
mid: NIHMS1680522
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Protein Kinase Inhibitors
0
Quinazolines
0
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
KDR protein, human
EC 2.7.10.1
Vascular Endothelial Growth Factor Receptor-2
EC 2.7.10.1
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
116061Subventions
Organisme : NCI NIH HHS
ID : R01 CA142868
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.
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