2-(3-Bromophenyl)-8-fluoroquinazoline-4-carboxylic acid as a novel and selective aurora A kinase inhibitory lead with apoptosis properties : design, synthesis, in vitro and in silico biological evaluation
Elsherbeny, Mohamed H. and Ammar, Usama M. and Abdellattif, Magda H. and Abourehab, Mohammed A. S. and Abdeen, Ahmed and Ibrahim, Samah F and Abdelrahaman, Doaa and Mady, Wessam and Roh, Eun Joo and Elkamhawy, Ahmed (2022) 2-(3-Bromophenyl)-8-fluoroquinazoline-4-carboxylic acid as a novel and selective aurora A kinase inhibitory lead with apoptosis properties : design, synthesis, in vitro and in silico biological evaluation. Life, 12 (6). 876. ISSN 2075-1729 (https://doi.org/10.3390/life12060876)
Preview |
Text.
Filename: Elsherbeny_etal_Life_2022_2_3_Bromophenyl_8_fluoroquinazoline_4_carboxylic_acid_as_a_novel_and_selective_aurora.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
New quinazoline derivatives were designed based on the structural modification of the reported inhibitors to enhance their selectivity toward Aurora A. The synthesized compounds were tested over Aurora A, and a cytotoxicity assay was performed over NCI cell lines to select the best candidate for further evaluation. Compound 6e (2‐(3‐bromophenyl)‐8‐fluoroquinazoline‐4‐ carboxylic acid) was the most potent compound among the tested derivatives. A Kinase panel assay was conducted for compound 6e over 14 kinases to evaluate its selectivity profile. Further cell cycle and apoptosis analysis were evaluated for compound 6e over the MCF‐7 cell line at its IC50 of 168.78 μM. It arrested the cell cycle at the G1 phase and induced apoptosis. Molecular docking was performed to explore the possible binding mode of compound 6e into the active site. It showed significant binding into the main pocket in addition to potential binding interactions with the key amino acid residues. Accordingly, compound 6e can be considered a potential lead for further structural and molecular optimization of the quinazoline‐based carboxylic acid scaffold for Aurora A kinase selective inhibition with apoptosis properties.
ORCID iDs
Elsherbeny, Mohamed H., Ammar, Usama M. ORCID: https://orcid.org/0000-0002-7218-641X, Abdellattif, Magda H., Abourehab, Mohammed A. S., Abdeen, Ahmed, Ibrahim, Samah F, Abdelrahaman, Doaa, Mady, Wessam, Roh, Eun Joo and Elkamhawy, Ahmed;-
-
Item type: Article ID code: 81569 Dates: DateEvent10 June 2022Published7 June 2022Accepted26 April 2022SubmittedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 26 Jul 2022 13:30 Last modified: 11 Nov 2024 13:33 URI: https://strathprints.strath.ac.uk/id/eprint/81569