Fatty Acid Conjugated Chalcones as Tubulin Polymerization Inhibitors: Design, Synthesis, QSAR, and Apoptotic and Antiproliferative Activity.
Tubulin Modulators
/ chemistry
Chalcones
/ pharmacology
Quantitative Structure-Activity Relationship
Tubulin
/ metabolism
Structure-Activity Relationship
Microtubules
/ metabolism
Antineoplastic Agents
/ chemistry
Cell Proliferation
Drug Screening Assays, Antitumor
Molecular Structure
Cell Line, Tumor
Journal
Journal of natural products
ISSN: 1520-6025
Titre abrégé: J Nat Prod
Pays: United States
ID NLM: 7906882
Informations de publication
Date de publication:
26 05 2023
26 05 2023
Historique:
medline:
29
5
2023
pubmed:
26
4
2023
entrez:
26
4
2023
Statut:
ppublish
Résumé
Cancer is often associated with an aberrant increase in tubulin and microtubule activity required for cell migration, invasion, and metastasis. A new series of fatty acid conjugated chalcones have been designed as tubulin polymerization inhibitors and anticancer candidates. These conjugates were designed to harness the beneficial physicochemical properties, ease of synthesis, and tubulin inhibitory activity of two classes of natural components. New lipidated chalcones were synthesized from 4-aminoacetophenone via
Identifiants
pubmed: 37098901
doi: 10.1021/acs.jnatprod.2c00793
doi:
Substances chimiques
Tubulin Modulators
0
Chalcones
0
Tubulin
0
Antineoplastic Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM