In vitro cytotoxic investigation of some synthesized 1,6-disubstituted-1-azacoumarin derivatives as anticancer agents

Aims: In this study, novel synthesized 1,6-disubstituted-1-azacoumarin-3-carboxylic acid derivatives were designed, synthesized and evaluated as potential anticancer agents. Materials & methods: The cytotoxicity of novel 1-azacoumarin-3-carboxylic acid derivatives was tested using an MTT assay. High potency was shown by DNA flow cytometry on MCF-7 cells for compound 3b. In addition, topoisomerase IIβ, caspase 3/7, Bax and Bcl-2 enzymes were used to study apoptotic activity. In the same studies, molecular docking analysis assessed activity. Results & conclusion: Cytotoxicity screening identified multiple bioactive compounds, especially compound 3b. Analysis of DNA flow cytometry revealed that compound 3b exhibited cell cycle arrest. Compound 3b had an increase in the expression of Bax/Bcl-2 ratio and caspase 3/7, and a decrease in topoisomerase IIβ enzyme inhibition.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:15

Enthalten in:

Future medicinal chemistry - 15(2023), 24 vom: 04. Dez., Seite 2289-2307

Sprache:

Englisch

Beteiligte Personen:

Ali Barakat, Lamiaa Abellatef [VerfasserIn]
El-Deen, Ibrahim Mohy [VerfasserIn]
El-Zend, Manar Abdo [VerfasserIn]
El-Behery, Mohammed [VerfasserIn]

Links:

Volltext

Themen:

803BHY7QWU
9007-49-2
Anticancer
Antineoplastic Agents
Azacoumarin
Bax/Bcl2
Bcl-2-Associated X Protein
Carbostyril
Carboxylic Acids
Caspase 3
Caspase 3/7
Cytotoxicity
DNA
Docking
EC 3.4.22.-
Journal Article
MCF-7
Proto-Oncogene Proteins c-bcl-2

Anmerkungen:

Date Completed 21.12.2023

Date Revised 21.12.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.4155/fmc-2023-0260

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM365383511