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Tideglusib

Catalog No. T3067   CAS 865854-05-3
Synonyms: NP-12, NP031112

Tideglusib (NP031112), a non-ATP competitive inhibitor of glycogen synthase kinase 3 (GSK-3), is with anti-inflammatory and neuroprotective activities.

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Tideglusib Chemical Structure
Tideglusib, CAS 865854-05-3
Pack Size Availability Price/USD Quantity
10 mg In stock $ 39.00
25 mg In stock $ 70.00
50 mg In stock $ 115.00
100 mg In stock $ 197.00
200 mg In stock $ 297.00
500 mg In stock $ 516.00
1 mL * 10 mM (in DMSO) In stock $ 43.00
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Purity: 99.84%
Purity: 99%
Purity: 98.89%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Tideglusib (NP031112), a non-ATP competitive inhibitor of glycogen synthase kinase 3 (GSK-3), is with anti-inflammatory and neuroprotective activities.
Targets&IC50 GSK-3β:60 nM
Kinase Assay [35S]Tideglusib (207 Bq/nmol) at 55 μM is incubated with 5 μM GSK-3β for 1 h at 25°C in 315 μL of 50 mM Tris-HCl, pH 7.5, containing 150 mM NaCl and 0.1 mM EGTA. The incubation is extended for another 30 min after having added 35 μL of the same buffer with or without 100 mM DTE. Samples are then processed in three different ways. First, an aliquot of 125 μL of each sample is mixed with 375 μL of 8 M GdnHCl in Water and heated at 80°C for 5 min. A second aliquot of 125 μL is diluted up to 500 μL with Water and left at room temperature for 5 min. In both cases, the free drug is removed afterwards by gel filtration through Sephadex G-25, and the amount of bound drug is determined by liquid scintillation counting on a 1450-MicroBeta TriLux counter. Finally, a third 40 μL aliquot of each original sample is mixed with 10 μL of denaturing electrophoresis sample buffer without reducing agents, and 35 μL of this mixture is loaded onto a 10% polyacrylamide gel and subjected to SDS-PAGE (again in the absence of reducing agents except for the DTE already included in the corresponding sample), followed by fluorography of the dried gel[1].
Synonyms NP-12, NP031112
Molecular Weight 334.39
Formula C19H14N2O2S
CAS No. 865854-05-3

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

Ethanol: < 1 mg/mL (insoluble or slightly soluble)

DMSO: >15 mg/mL(44.9 mM)

TargetMolReferences and Literature

1. Domínguez JM, et al. J Biol Chem, 2012, 287(2), 893-90 2. Luna-Medina R, et al. J Neurosci, 2007, 27(21), 5766-5776. 3. Serenó L, et al. Neurobiol Dis, 2009, 35(3), 359-367.

TargetMolCitations

1. Dou X, Sun Q, Xu G, et al. Discovery of 2-(furan-2-ylmethylene) hydrazine-1-carbothioamide derivatives as novel inhibitors of SARS-CoV-2 main protease. European Journal of Medicinal Chemistry. 2022: 114508

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library Highly Selective Inhibitor Library Inhibitor Library Anti-Cancer Clinical Compound Library Kinase Inhibitor Library FDA-Approved Kinase Inhibitor Library Anti-Cancer Drug Library Anti-Neurodegenerative Disease Compound Library Anti-Cancer Active Compound Library Anti-Cancer Approved Drug Library

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Keywords

Tideglusib 865854-05-3 PI3K/Akt/mTOR signaling Stem Cells GSK-3 Glycogen synthase kinase-3 NP 031112 NP-12 NP 12 inhibit Glycogen synthase kinase 3 NP12 Inhibitor NP-031112 NP031112 inhibitor

 

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