Elraglusib GSK-3 inhibitor

Cat.No.S9602

Elraglusib(9-ING-41) is a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with antitumor activity. 9-ING-41 induces apoptosis and cell cycle arrest at prophase by targeting centrosomes and microtubule-bound GSK3β.
Elraglusib GSK-3 inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 404.35

Quality Control

Batch: S960201 DMSO]81 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 99.63%
99.63

Chemical Information, Storage & Stability

Molecular Weight 404.35 Formula

C22H13FN2O5

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1034895-42-5 -- Storage of Stock Solutions

Synonyms 9-ing-41 Smiles CN1C=C(C2=CC3=C(C=C21)OCO3)C4=C(C(=O)NC4=O)C5=COC6=C5C=C(C=C6)F

Solubility

In vitro
Batch:

DMSO : 81 mg/mL (200.32 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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In vivo Formulation Calculator (Clear solution)

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Mechanism of Action

Targets/IC50/Ki
GSK-3 [1]
In vitro

9-ING-41, a clinically relevant small molecule GSK-3β inhibitor with broad spectrum pre-clinical antitumor activity, suppresses the growth of neuroblastoma cells.[1] 9-ING-41 induces apoptosis and cell cycle arrest at prophase by targeting centrosomes and microtubule-bound GSK3β.[2]

In vivo

9-ING-41 has single-agent antitumor activity in a mouse model of MCL.[2] Mouse xenograft studies shows that the combination of clinically relevant doses of CPT-11 and 9-ING-41 lead to greater antitumor effect than is observed with either agent alone.[1]

References

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