Synthesis, In Silico and In Vitro Assessment of New Quinazolinones as Anticancer Agents via Potential AKT Inhibition
A series of novel quinazolinone derivatives (<b>2</b>–<b>13</b>) was synthesized and examined for their cytotoxicity to HepG2, MCF-7, and Caco-2 in an MTT assay. Among these derivatives, compounds <b>4</b> and <b>9</b> exhibited significant cytotoxic a...
Main Authors: | Ahmed A. Noser, Mohamed El-Naggar, Thoria Donia, Aboubakr H. Abdelmonsef |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-10-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/25/20/4780 |
Similar Items
-
Synthesis and cytotoxic evaluation of novel quinazolinone derivatives as potential anticancer agents
by: Safoora Poorirani, et al.
Published: (2018-01-01) -
Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents
by: Fahimeh Taayoshi, et al.
Published: (2022-05-01) -
Synthesis of some quinazolinones inspired from the natural alkaloid L-norephedrine as EGFR inhibitors and radiosensitizers
by: Mostafa M. Ghorab, et al.
Published: (2021-01-01) -
Synthesis, Cytotoxic Evaluation, and Structure-Activity Relationship of Substituted Quinazolinones as Cyclin-Dependent Kinase 9 Inhibitors
by: Hamad M. Alkahtani, et al.
Published: (2022-12-01) -
Synthesis and cytotoxic evaluation of some derivatives of triazole-quinazolinone hybrids
by: Farshid Hassanzadeh, et al.
Published: (2019-01-01)