864686-48-6
Chemical Structure
BI-5521
- CAS No.: 864686-48-6
- Formula:C24H25N3O4
- Molecular Weight:419.47
InChIKey: VLYNCWZASZUTNV-FCQUAONHSA-N
SMILES: O=C(/C1=C(NC2CCN(C)CC2)/C3=CC(OCO4)=C4C=C3)NC5=C1C=C(C(C)=O)C=C5
Biological Activity: BI-5521 is an orally active GSK-3 inhibitor with an IC50 of 1.1 nM against GSK-3β. BI-5521 targets the two GSK-3 isoforms with similar potency and exhibits potent inhibitory activity against DYRK1A. By modulating GSK-3 activity, BI-5521 inhibits tumor proliferation and cancer cell growth, exerts cytotoxic effects, and reduces cancer cell viability. It shows consistent chemosensitivity across all subtypes of rhabdomyosarcoma, produces synergistic growth inhibitory effects when combined with SOS1 inhibitors, reduces oral glucose levels, regulates the myofibroblast differentiation pathway, decreases the nuclear localization of YAP/SMAD2/3, and lowers the positive rate of α-SMA in fibroblasts without affecting the apoptosis of CD4+ T cells. BI-5521 can be used in the research of non-small cell lung cancer, pleomorphic rhabdomyosarcoma, type 2 diabetes, pancreatic ductal adenocarcinoma, Alzheimer's disease, bipolar disorder, and metabolic dysfunction-associated steatotic liver disease[1][2][3][4][5][6].
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BI-5521 | BI-5521 is an orally active GSK-3 inhibitor with an IC50 of 1.1 nM against GSK-3β. BI-5521 targets the two GSK-3 isoforms with similar potency and exhibits potent inhibitory activity against DYRK1A. By modulating GSK-3 activity, BI-5521 inhibits tumor proliferation and cancer cell growth, exerts cytotoxic effects, and reduces cancer cell viability. It shows consistent chemosensitivity across all subtypes of rhabdomyosarcoma, produces synergistic growth inhibitory effects when combined with SOS1 inhibitors, reduces oral glucose levels, regulates the myofibroblast differentiation pathway, decreases the nuclear localization of YAP/SMAD2/3, and lowers the positive rate of α-SMA in fibroblasts without affecting the apoptosis of CD4+ T cells. BI-5521 can be used in the research of non-small cell lung cancer, pleomorphic rhabdomyosarcoma, type 2 diabetes, pancreatic ductal adenocarcinoma, Alzheimer's disease, bipolar disorder, and metabolic dysfunction-associated steatotic liver disease. | |||||||||||||||||||||
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- [1]. Hamilton G, et al. Characterization of the BH1406 non-small cell lung cancer (NSCLC) cell line carrying an activating SOS1 mutation. Translational lung cancer research. 2024 Nov 30;13(11):2987-2997. [Content Brief]
- [2]. Stickler S, et al. Characterization of a pleomorphic rhabdomyosarcoma cell line. Scientific reports. 2025 Jan 23;15(1):2893. [Content Brief]
- [3]. Gollner A, et al. Kinase Degraders, Activators, and Inhibitors: Highlights and Synthesis Routes to the Chemical Probes on opnMe.com, Part 1. ChemMedChem. 2023 May 16;18(10):e202300031. [Content Brief]
- [4]. Ercin M, et al. Exploring the role of cellular plasticity in metabolic dysfunction-associated steatosis and related molecular mechanisms. Journal of translational medicine. 2025 Nov 13;23(1):1278. [Content Brief]
- [5]. Tanaka HY, et al. Heterotypic 3D pancreatic cancer model with tunable proportion of fibrotic elements. Biomaterials. 2020 Aug;251:120077. [Content Brief]
- [6]. Bonaguro L, et al. CRELD1 modulates homeostasis of the immune system in mice and humans. Nature immunology. 2020 Dec;21(12):1517-1527. [Content Brief]
Keywords