GSK-3β inhibitor 3
CAS No. 1448990-73-5
GSK-3β inhibitor 3( —— )
Catalog No. M34769 CAS No. 1448990-73-5
GSK-3β inhibitor 3 is a potent, selective, and irreversible covalent inhibitor of glycogen synthase kinase 3β (GSK-3β) with an IC50 of 6.6 μM, and can be used to study acute promyelocytic leukemia.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 128 | In Stock |
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| 5MG | 188 | In Stock |
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| 10MG | 282 | In Stock |
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| 25MG | 513 | In Stock |
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| 50MG | 769 | In Stock |
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| 100MG | 1107 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameGSK-3β inhibitor 3
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NoteResearch use only, not for human use.
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Brief DescriptionGSK-3β inhibitor 3 is a potent, selective, and irreversible covalent inhibitor of glycogen synthase kinase 3β (GSK-3β) with an IC50 of 6.6 μM, and can be used to study acute promyelocytic leukemia.
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DescriptionGSK-3β inhibitor 3 is a potent, selective, irreversible and covalent inhibitor of Glycogen Synthase Kinase 3β (GSK-3β), with an IC50 of 6.6 μM. GSK-3β inhibitor 3 can be used for the research of acute promyelocytic leukemia.
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In VitroGSK-3β inhibitor 3 (compound 4-3) (100 μM) inhibits GSK-3α activity by 87.3%.GSK-3β inhibitor 3 (6.25-100 μM; 24-48 h) dose-dependently inhibits the growth of NB4 and NB4-R1 cells.GSK-3β inhibitor 3 (12.5-100 μM; 24 h) significantly increases the percentage of apoptosis in a dose-dependent pattern in NB4 and NB4-R1 cells.Cell Viability Assay Cell Line:NB4 and NB4-R1 cells Concentration:6.25, 12.5, 25, 50, 100 μM Incubation Time:24, 48 hours Result:Inhibited the cell viability, with IC50s of 19.56 μM and 26.42 μM in NB4 and NB4-R1 cells at 24 h, respectively.Had little cytotoxicity on human normal liver cells (LO2) and human umbilical vein endothelial cells (HUVECs).Apoptosis Analysis Cell Line:NB4 and NB4-R1 cells Concentration:12.5, 25, 50, 100 μM Incubation Time:24 hours Result:Induced cell apoptosis.
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In VivoGSK-3β inhibitor 3 (compound 4-3) (15 mg/kg/d; i.p. for 2 weeks) inhibits tumor growth of mice by 75.97% relative to vehicle control.GSK-3β inhibitor 3 (15 mg/kg; a single i.p.) shows long T1/2 of 14.2 h, high AUC values (AUClast=3503.42 ng/mL?h), and maximum concentration (Cmax=515 ng/mL) in mice.Animal Model:Balb/c female nude mice were injected leukemia cellsDosage:15 mg/kg/d Administration:I.p. for 2 weeks Result: Inhibited localized growth in NB4 cells.Had mild weight loss compared with control.Animal Model:Male ICR mice (30 g) Dosage:15 mg/kg (Pharmacokinetic Analysis) Administration:A single i.p.Result:T1/2=14.2 h; AUClast=3503.42 ng/mL?h; Cmax=515 ng/mL.
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Synonyms——
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PathwayApoptosis
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TargetApoptosis
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RecptorApoptosis | GSK-3
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Research Area——
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Indication——
Chemical Information
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CAS Number1448990-73-5
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Formula Weight327.37
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Molecular FormulaC18H14FNO2S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (763.66 mM; Ultrasonic )
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SMILESFc1ccc(cc1)C1CC(=O)N(C(=O)C=C)c2ccccc2S1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Zhang P, et, al. Discovery of Novel Benzothiazepinones as Irreversible Covalent Glycogen Synthase Kinase 3β Inhibitors for the Treatment of Acute Promyelocytic Leukemia. J Med Chem. 2021 May 24.?
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