Imidazopyridine-based kinase inhibitors as potential anticancer agents : A review

Copyright © 2023 Elsevier Inc. All rights reserved..

Considering the fundamental role of protein kinases in the mechanism of protein phosphorylation in critical cellular processes, their dysregulation, especially in cancers, has underscored their therapeutic relevance. Imidazopyridines represent versatile scaffolds found in abundant bioactive compounds. Given their structural features, imidazopyridines have possessed pivotal potency to interact with different protein kinases, inspiring researchers to carry out numerous structural variations. In this comprehensive review, we encompass an extensive survey of the design and biological evaluations of imidazopyridine-based small molecules as potential agents targeting diverse kinases for anticancer applications. We describe the structural elements critical to inhibitory potency, elucidating their key structure-activity relationships (SAR) and mode of actions, where available. We classify these compounds into two groups: Serine/threonine and Tyrosine inhibitors. By highlighting the promising role of imidazopyridines in kinase inhibition, we aim to facilitate the design and development of more effective, targeted compounds for cancer treatment.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:140

Enthalten in:

Bioorganic chemistry - 140(2023) vom: 15. Nov., Seite 106831

Sprache:

Englisch

Beteiligte Personen:

Peytam, Fariba [VerfasserIn]
Emamgholipour, Zahra [VerfasserIn]
Mousavi, Alireza [VerfasserIn]
Moradi, Mahfam [VerfasserIn]
Foroumadi, Roham [VerfasserIn]
Firoozpour, Loghman [VerfasserIn]
Divsalar, Fatemeh [VerfasserIn]
Safavi, Maliheh [VerfasserIn]
Foroumadi, Alireza [VerfasserIn]

Links:

Volltext

Themen:

Antineoplastic Agents
Cancer
Imidazoles
Imidazopyridine
Journal Article
Kinase
Pyridines
Research Support, Non-U.S. Gov't
Review

Anmerkungen:

Date Completed 18.09.2023

Date Revised 18.09.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.bioorg.2023.106831

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM361810636