SKI 178 |
| Catalog No.GC44896 |
SKI 178 es un potente inhibidor de la esfingosina quinasa-1 (SphK1) y SphK2. SKI 178 es citotóxico en concentraciones IC50 que van desde 1,8 a 0,1 μM en líneas celulares de cáncer sensibles a fármacos y resistentes a múltiples fármacos (es decir, células MTR3, NCI-ADR y HL60/VCR). SKI 178 induce la apoptosis de manera dependiente de CDK1 en líneas celulares de leucemia mieloide aguda humana.
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Cas No.: 1259484-97-3
Sample solution is provided at 25 µL, 10mM.
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SKI 178 is an inhibitor of sphingosine kinase 1 (SPHK1) and SPHK2. Though previously thought to be selective for SPHK1, cellular thermal shift assay results demonstrate direct target engagement of both SPHK1 and SPHK2 in HEK293 cells overexpressing either SPHK1 or SPHK2. It inhibits SPHK1 by 59.6% when used at a concentration of 10.7 µM and inhibits the production of sphingosine-1-phosphate in A549 cells. SKI 178 is cytotoxic to a variety of cancer cell lines including PANC-1, A549, U251, and MCF-7 cells (IC50s = 0.1, 0.3, 0.5, and 1.3 µM, respectively). It prolongs mitosis and induces cell death through the intrinsic apoptotic pathway in a CDK1-dependent manner. SKI 178 (20 mg/kg every other day) reduces the number of white blood cells to a normal range and increases survival in an MLL-AF9 acute myeloid leukemia (AML) mouse xenograft model. It also destabilizes and inhibits microtubule polymerization in an SPHK-independent manner.
Average Rating: 5 (Based on Reviews and 13 reference(s) in Google Scholar.)
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