For research use only. Not for therapeutic Use.
CP21R7(CAT: I001003) is a potent and selective inhibitor of Glycogen Synthase Kinase-3 Beta (GSK-3β), a serine/threonine kinase involved in regulating various cellular processes, including cell proliferation, apoptosis, and metabolism. By inhibiting GSK-3β, CP21R7 modulates key signaling pathways such as the Wnt/β-catenin and PI3K/Akt pathways, which are often dysregulated in diseases like cancer, neurodegenerative disorders, and diabetes. Its high selectivity makes it a valuable compound in oncology and neurological research, providing insights into therapeutic strategies for conditions driven by abnormal GSK-3β activity, including Alzheimer’s disease, bipolar disorder, and tumor progression.
Catalog Number | I001003 |
CAS Number | 125314-13-8 |
Synonyms | 3-(3-aminophenyl)-4-(1-methyl-1H-indol-3-yl)-1H-pyrrole-2,5-dione |
Molecular Formula | C₁₉H₁₅N₃O₂ |
Purity | ≥95% |
Target | Stem Cell/Wnt |
Solubility | DMSO: ≥ 34 mg/mL |
Storage | Store at -20°C |
IUPAC Name | 3-(3-aminophenyl)-4-(1-methylindol-3-yl)pyrrole-2,5-dione |
InChI | InChI=1S/C19H15N3O2/c1-22-10-14(13-7-2-3-8-15(13)22)17-16(18(23)21-19(17)24)11-5-4-6-12(20)9-11/h2-10H,20H2,1H3,(H,21,23,24) |
InChIKey | RGTAEYDIDMGJLX-UHFFFAOYSA-N |
SMILES | CN1C=C(C2=CC=CC=C21)C3=C(C(=O)NC3=O)C4=CC(=CC=C4)N |