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.
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- CAS No.: 2380013-55-6
- Formule: C17H18N4O2S
- Masse moléculaire:342.42
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
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.
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Cell Line:C3H10T1/2 mesenchymal progenitor cells
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Concentration:0.001, 0.01, 0.1, 1, 10 μM
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Incubation Time:96 h
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Result:Potently inhibited Purmorphamine-induced osteogenesis, with an IC50 of 0.6 μM.
Chemical Information
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CAS No. 2380013-55-6
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Masse moléculaire 342.42
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Formule C17H18N4O2S
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SMILES
O=C(C1=CC=C(NC2=NC(NC(C)C)=NC3=C2SC=C3)C=C1)OC
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)