الصفحة الرئيسية>>Signaling Pathways>> Stem Cell>> Wnt/β-catenin>>SKI II

SKI II (Synonyms: SKI II, SPHK I2)

رقم الكتالوجGC16701

SKI-II هو مثبط نشط ومُصنَّع عن طريق الفم لنشاط sphingosine kinase (SK) ، مع قيم IC تبلغ 78 ميكرومتر و 45 ميكرومتر لـ SK1 و SK2 ، على التوالييتسبب SKI II في تثبيط لا رجعة فيه لـ SK1 عن طريق تحفيز تحللها الليزوزومي و / أو البروتوزوم

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SKI II التركيب الكيميائي

Cas No.: 312636-16-1

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
41٫00
متوفر
25mg
70٫00
متوفر
100mg
253٫00
متوفر
500mg
1112٫00
متوفر
1g
1916٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

SKI II is an inhibitor of sphingosine kinase with IC50 value of 0.5μM[1].

SKI II is selective against SK and has no inhibition of human protein kinases ERK2, PKC-I and the lipid kinase PI3K. It is reported that SKI II is not a competitive inhibitor at the ATP-binding site of SK. SKI II also inhibits endogenous SK in intact MDA-MB-231 cells [1].

As a SK inhibitor, SKI II prevents SK from catalyzing the generation of sphingosine 1-phosphate (S1P). The blockage of S1P formation leads to inhibition of proliferation, as well as the induction of apoptosis in cancer cells. SKI II shows cytotoxicity in T-24 human bladder carcinoma cells, MCF-7 human breast adenocarcinoma cells and the subline of MCF-7 cells, MCF-7/VP, with IC50 values of 4.6μM, 1.2μM and 0.9μM, respectively [1].

References:
[1] French KJ, Schrecengost RS, Lee BD, Zhuang Y, Smith SN, Eberly JL, Yun JK, Smith CD. Discovery and evaluation of inhibitors of human sphingosine kinase. Cancer Res. 2003 Sep 15;63(18):5962-9.

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