1. PI3K/Akt/mTOR Stem Cell/Wnt
  2. PI4K Hedgehog
  3. Pipinib

Pipinib is an ATP-competitive and selective phosphatidylinositol 4-kinase IIIb (PI4KB) inhibitor with an IC50 of 2.2 μM. Pipinib reduces intracellular PI4P levels. Pipinib inhibits GLI-mediated transcription, the expression of Hedgehog target genes, and blocks the trafficking of Smoothened to cilia. Pipinib can be used in the research of basal cell carcinoma and medulloblastoma.

For research use only. We do not sell to patients.

Pipinib

Pipinib Chemical Structure

CAS No. : 2380013-55-6

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Description

Pipinib is an ATP-competitive and selective phosphatidylinositol 4-kinase IIIb (PI4KB) inhibitor with an IC50 of 2.2 μM. Pipinib reduces intracellular PI4P levels. Pipinib inhibits GLI-mediated transcription, the expression of Hedgehog target genes, and blocks the trafficking of Smoothened to cilia. Pipinib can be used in the research of basal cell carcinoma and medulloblastoma[1].

In Vitro

Pipinib (0.001-10 μM; 96 h) inhibits Purmorphamine (HY-15108)-induced osteogenesis in C3H10T1/2 cells, with an IC50 of 0.6 μM[1].
Pipinib (0.01-100 μM; 48 h) inhibits GLI-mediated transcription in Shh-LIGHT2 cells, with an IC50 of 1.7 μM[1].
Pipinib (0.01-10 μM; 48 h) reduces the Purmorphamine-induced expression of Ptch1 and Gli1 in NIH/3T3 cells, with IC50 values of 3.1 μM and 4.1 μM, respectively[1].
Pipinib (5 μM; 48 h) reduces PI4P levels in NIH/3T3 cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Differentiation Assay[1]

Cell Line: C3H10T1/2 mesenchymal progenitor cells
Concentration: 0.001, 0.01, 0.1, 1, 10 μM
Incubation Time: 96 h
Result: Potently inhibited Purmorphamine-induced osteogenesis, with an IC50 of 0.6 μM.
Molecular Weight

342.42

Formula

C17H18N4O2S

CAS No.
SMILES

O=C(C1=CC=C(NC2=NC(NC(C)C)=NC3=C2SC=C3)C=C1)OC

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Purity & Documentation
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Pipinib
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HY-182721
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