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Advances in the discovery of activin receptor-like kinase 5 (ALK5) inhibitors.
- Source :
-
Bioorganic chemistry [Bioorg Chem] 2024 Jun; Vol. 147, pp. 107332. Date of Electronic Publication: 2024 Apr 03. - Publication Year :
- 2024
-
Abstract
- Activin receptor‑like kinase-5 (ALK5) is an outstanding member of the transforming growth factor-β (TGF-β) family. (TGF-β) signaling pathway integrates pleiotropic proteins that regulate various cellular processes such as growth, proliferation, and differentiation. Dysregulation within the signaling pathway can cause variety of diseases, such as fibrosis, cardiovascular disease, and especially cancer, rendering ALK5 a potential drug target. Hence, various small molecules have been designed and synthesized as potent ALK5 inhibitors. In this review, we shed light on the current ATP-competitive inhibitors of ALK5 through diverse heterocyclic based scaffolds that are in clinical or pre-clinical phases of development. Moreover, we focused on the binding interactions of the compounds to the ATP binding site and the structure-activity relationship (SAR) of each scaffold, revealing new scopes for designing novel candidates with enhanced selectivity and metabolic profiles.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Humans
Structure-Activity Relationship
Molecular Structure
Animals
Protein Kinase Inhibitors pharmacology
Protein Kinase Inhibitors chemistry
Protein Kinase Inhibitors chemical synthesis
Receptor, Transforming Growth Factor-beta Type I antagonists & inhibitors
Receptor, Transforming Growth Factor-beta Type I metabolism
Drug Discovery
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2120
- Volume :
- 147
- Database :
- MEDLINE
- Journal :
- Bioorganic chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 38581966
- Full Text :
- https://doi.org/10.1016/j.bioorg.2024.107332