Design, synthesis and biological evaluation of quinoline-2-carbonitrile-based hydroxamic acids as dual tubulin polymerization and histone deacetylases inhibitors.
Antineoplastic Agents
Cell Line, Tumor
Cell Proliferation
Drug Design
Drug Screening Assays, Antitumor
Histone Deacetylase Inhibitors
/ pharmacology
Histone Deacetylases
/ metabolism
Humans
Hydroxamic Acids
/ pharmacology
Polymerization
Quinolines
/ pharmacology
Repressor Proteins
Tubulin
/ metabolism
Cancer
Cytotoxicity
HDACi
Multitargeted compounds
Tubulin
Journal
European journal of medicinal chemistry
ISSN: 1768-3254
Titre abrégé: Eur J Med Chem
Pays: France
ID NLM: 0420510
Informations de publication
Date de publication:
05 Oct 2022
05 Oct 2022
Historique:
received:
07
04
2022
revised:
23
06
2022
accepted:
24
06
2022
pubmed:
8
7
2022
medline:
17
8
2022
entrez:
7
7
2022
Statut:
ppublish
Résumé
A series of quinoline and quinazoline analogs were designed and synthesized as new tubulin polymerization (TP) and histone deacetylases (HDAC) inhibitors. Compounds 12a and 12d showed the best cytotoxicity activities against a panel of human cancer cell lines with an averaged IC
Identifiants
pubmed: 35797900
pii: S0223-5234(22)00475-5
doi: 10.1016/j.ejmech.2022.114573
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Histone Deacetylase Inhibitors
0
Hydroxamic Acids
0
Quinolines
0
Repressor Proteins
0
Tubulin
0
HDAC8 protein, human
EC 3.5.1.98
Histone Deacetylases
EC 3.5.1.98
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
114573Informations de copyright
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