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Scaffold Repurposing of In-House Small Molecule Candidates Leads to Discovery of First-in-Class CDK-1/HER-2 Dual Inhibitors: In Vitro and In Silico Screening

Elkamhawy, Ahmed; Ammar, Usama; Paik, Sora; Abdellattif, Magda H.; Elsherbeny, Mohamed H.; Lee, Kyeong; Joo Roh, Eun

Authors

Ahmed Elkamhawy

Sora Paik

Magda H. Abdellattif

Mohamed H. Elsherbeny

Kyeong Lee

Eun Joo Roh



Abstract

Recently, multitargeted drugs are considered a potential approach in treating cancer. In this study, twelve in-house indole-based derivatives were preliminary evaluated for their inhibitory activities over VEGFR-2, CDK-1/cyclin B and HER-2. Compound 15l showed the most inhibitory activities among the tested derivatives over CDK-1/cyclin B and HER-2. Compound 15l was tested for its selectivity in a small kinase panel. It showed dual selectivity for CDK-1/cyclin B and HER-2. Moreover, in vitro cytotoxicity assay was assessed for the selected series against nine NCI cell lines. Compound 15l showed the most potent inhibitory activities among the tested compounds. A deep in silico molecular docking study was conducted for compound 15l to identify the possible binding modes into CDK-1/cyclin B and HER-2. The docking results revealed that compound 15l displayed interesting binding modes with the key amino acids in the binding sites of both kinases. In vitro and in silico studies demonstrate the indole-based derivative 15l as a selective dual CDK-1 and HER-2 inhibitor. This emphasizes a new challenge in drug development strategies and signals a significant milestone for further structural and molecular optimization of these indole-based derivatives in order to achieve a drug-like property.

Citation

Elkamhawy, A., Ammar, U., Paik, S., Abdellattif, M. H., Elsherbeny, M. H., Lee, K., & Joo Roh, E. (2021). Scaffold Repurposing of In-House Small Molecule Candidates Leads to Discovery of First-in-Class CDK-1/HER-2 Dual Inhibitors: In Vitro and In Silico Screening. Molecules, 26(17), Article 5324. https://doi.org/10.3390/molecules26175324

Journal Article Type Article
Acceptance Date Aug 30, 2021
Online Publication Date Sep 1, 2021
Publication Date Sep 1, 2021
Deposit Date Dec 11, 2022
Publicly Available Date Dec 12, 2022
Journal Molecules
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 26
Issue 17
Article Number 5324
DOI https://doi.org/10.3390/molecules26175324
Keywords CDK-1/cyclin B; HER-2; anti-proliferative; anti-cancer; molecular docking; drug repurposing
Public URL http://researchrepository.napier.ac.uk/Output/2973652

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