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TCS 2002

TCS 2002
GSK-3β inhibitor 9 (Compound 9b) is a highly selective, orally bioavailable and potent GSK-3β inhibitor with the IC 50 of 35 nM. GSK-3β inhibitor 9 exhibits good pharmacokinetic profiles including favorable BBB penetration. GSK-3β inhibitor 9 is able to be used for the research of Alzheimer’s disease [1].
Catalog No. T22157Cas No. 1005201-24-0

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TCS 2002

Catalog No. T22157Cas No. 1005201-24-0

GSK-3β inhibitor 9 (Compound 9b) is a highly selective, orally bioavailable and potent GSK-3β inhibitor with the IC 50 of 35 nM. GSK-3β inhibitor 9 exhibits good pharmacokinetic profiles including favorable BBB penetration. GSK-3β inhibitor 9 is able to be used for the research of Alzheimer’s disease [1].
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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50 mg$2,66035 days
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Product Introduction

Bioactivity
Description
GSK-3β inhibitor 9 (Compound 9b) is a highly selective, orally bioavailable and potent GSK-3β inhibitor with the IC 50 of 35 nM. GSK-3β inhibitor 9 exhibits good pharmacokinetic profiles including favorable BBB penetration. GSK-3β inhibitor 9 is able to be used for the research of Alzheimer’s disease [1].
In vivo
GSK-3β inhibitor 9 (Compound 9b) exhibited potent pharmacokinetic properties when administered to GS rats and C57BL/6N mice at doses ranging from 1-3 mg/kg over periods of 1-24 hours. It demonstrated favorable blood-brain barrier (BBB) permeability, indicated by an AUC (area under the curve) 0-24h value of 734 ng•h/g and a brain-to-plasma ratio (Kp value) of 1.6. In experiments utilizing 8-week-old male IGS rats, Compound 9b was administered intravenously and orally at dosages of 1 and 3 mg/kg across various time points (1, 2, 4, 8, 24 hours). This treatment resulted in a volume of distribution (Vdss,iv) ranging from 1134 to 1650 mL/kg, total clearance (CLtotal,iv) between 27.4 and 28.4 mL/min/kg, and a maximum concentration (Cmax,po) from 289.6 to 396.9 ng/mL. Additionally, oral administration led to AUC 0-24 h values between 1229.1 and 1380.6 ng•h/mL, mean residence time (MRTpo) from 2.19 to 3.03 hours, and fraction dosed (Fd%) from 65.5 to 72.8%.
Chemical Properties
Molecular Weight338.38
FormulaC18H14N2O3S
Cas No.1005201-24-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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