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IWR-1-endo

IWR-1 (IWR-1-endo) is a novel small-molecule inhibitor of Wnt signaling by stabilizing the Axin destruction complex with an EC50 of 0.2 uM. (In Vitro) :Both IWR-1 and XAV939 act as reversible Wnt pathway inhibitors and exhibit similar pharmacological effects in vitro. IWR-1 exerts its effect via interaction with Axin, while XAV939 binds TNKS directly. IWR-1 (10 μM) induces stabilization of β-catenin disruption complex. IWR-1 (10 μM) is added to the medium together with MIF, the size of cell colonies is extremely decreased, and that indicates the promoting effect of MIF on NSPC proliferation is inhibited by IWR-1 in any MIF concentration group. 2, 5 and 10 μM of IWR-1 significantly inhibits the proliferation of NSPC dose-dependently. IWR-1 inhibites the promoting effect of MIF on NSPC differentiation to neuron lineage. IWR-1 treatment in the presence of maximal stimulatory dose of FSH (0.5 ng/mL) results in a dose dependent inhibition of the stimulatory effect of FSH with > 75% inhibition observed at the maximal inhibitory dose of IWR-1 (1 μM) . IWR-1 treatment partially reverses the FSH-induced inhibition of granulosa cell CARTPT mRNA expression.

Product Specifications

CAS Number

1127442-82-3

Product Name Alternative

IWR-1 | IWR 1 | IWR1 | IWR-1-endo.

Purity

>98% (HPLC)

Solubility

DMSO: 30 mg/mL (73.27 mM)

Smiles

O=C (NC1=C2N=CC=CC2=CC=C1) C3=CC=C (N (C (C4C (C5) C=CC5C64) =O) C6=O) C=C3

Molecular Formula

C25H19N3O3

Molecular Weight

409.44

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

4-[ (3aR,4S,7R,7aS) -1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl]-N-8-quinolinyl-benzamide

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