Evaluation of the cytotoxic, apoptosis inducing activity and molecular docking of spiroquinazolinone benzamide derivatives in MCF-7 breast cancer cells

M Mahdavi, MM Lavi, R Yekta, MA Moosavi… - Chemico-biological …, 2016 - Elsevier
Previous studies have suggested that quinazolinone derivatives are potent apoptosis-
inducing agents in various cancer cell lines. In the present study, we have investigated …

Spiroquinazolinone-induced cytotoxicity and apoptosis in K562 human leukemia cells: alteration in expression levels of Bcl-2 and Bax

M Ghasemian, M Mahdavi, P Zare… - The Journal of …, 2015 - jstage.jst.go.jp
Spiroquinazolinone compounds have been considered as a new series of potent apoptosis-
inducing agents. In this study, anti-proliferative and apoptotic effects of the derivatives from …

Novel sulphonamide-bearing methoxyquinazolinone derivatives as anticancer and apoptosis inducers: synthesis, biological evaluation and in silico studies

AS Alqahtani, MM Ghorab, FA Nasr… - Journal of Enzyme …, 2022 - Taylor & Francis
We synthesised a new series of sulphonamide-bearing quinazolinone derivatives 5-18 and
evaluated their in vitro cytotoxicity in various cancer cell lines (A549, HepG-2, LoVo and …

Design, synthesis and biological evaluation of some novel quinazolinone derivatives as potent apoptotic inducers

RM Nowar, EE A Osman, SM Abou-Seri… - Future Medicinal …, 2018 - Future Science
Aim: Novel quinazolinone and triazinoquinazolinone derivatives were designed and
synthesized as apoptotic inducers. Methodology/results: Most of the synthesized compounds …

Synthesis and evaluation of new 4 (3H)-Quinazolinone derivatives as potential anticancer agents

S Gatadi, G Pulivendala, J Gour, S Malasala… - Journal of Molecular …, 2020 - Elsevier
A series of new 4 (3H)-quinazolinones were synthesized and evaluated for their cytotoxic
activity against a set of human cancer cell lines MDA-MB-231 and MCF-7 (breast), HCT-116 …

In vitro anticancer evaluation of some synthesized 2H-quinolinone and halogenated 2H-quinolinone derivatives as therapeutic agents

RMA El-Aziz, I Zaki, IM El-Deen… - Anti-Cancer Agents …, 2020 - ingentaconnect.com
Background: Searching for new cytotoxic agents with apoptosis induction may represent a
viable strategy for cancer treatment to overcome the increased resistance to available …

[HTML][HTML] The antiproliferative and apoptotic effects of a novel quinazoline carrying substituted-sulfonamides: In vitro and molecular docking study

AS Alqahtani, MM Ghorab, FA Nasr, MZ Ahmed… - Molecules, 2022 - mdpi.com
In order to investigate for a new effective and safe anticancer drug, we synthesized a novel
series of quinazoline containing biologically active substituted-sulfonamide moiety at 3 …

[HTML][HTML] Synthesis, characterization and apoptotic activity of quinazolinone Schiff base derivatives toward MCF-7 cells via intrinsic and extrinsic apoptosis pathways

M Zahedifard, F Lafta Faraj, M Paydar, C Yeng Looi… - Scientific reports, 2015 - nature.com
The current study investigated the cytotoxic effect of 3-(5-chloro-2-hydroxybenzylideneamino
)-2-(5-chloro-2-hydroxyphenyl)-2, 3-dihydroquinazolin-41 (H)-one (A) and 3-(5-nitro-2 …

A novel quinazolinone chalcone derivative induces mitochondrial dependent apoptosis and inhibits PI3K/Akt/mTOR signaling pathway in human colon cancer HCT …

ZA Wani, SK Guru, AVS Rao, S Sharma… - Food and Chemical …, 2016 - Elsevier
We have synthesized a novel quinazolinone chalcone derivative (QC) and first time reported
its in-vitro and in-vivo anticancer potential. It inhibited the cell proliferation of different cancer …

Piperine derivatives as potential inhibitors of Survivin: An in silico molecular docking

E Sattarinezhad, AK Bordbar, N Fani - Computers in biology and medicine, 2015 - Elsevier
Targeting Survivin, as an inhibitor of apoptosis and a regulator of cell division, has become a
worldwide controversial issue. Piperine as a pungent alkaloid has been identified as the …