567726
D-erythro-Sphingosine, Free Base, High Purity
Highly purified preparation of bovine brain sphingosine containing >99% of the erythro isomer.
别名:
D-erythro-Sphingosine, Free Base, High Purity, Cerebroside, trans-D- erythro-2-Amino-4-octadecene-1,3-diol, Ceramide, Cerebroside, trans-D-erythro-2-Amino-4-octadecene-1,3-diol, Ceramide
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About This Item
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品質等級
化驗
≥98% (TLC)
形狀
solid
製造商/商標名
Calbiochem®
儲存條件
OK to freeze
顏色
white
溶解度
chloroform: 1 mg/mL
methanol: 1 mg/mL
DMSO: 10 mg/mL
運輸包裝
ambient
儲存溫度
−20°C
InChI
1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h14-15,17-18,20-21H,2-13,16,19H2,1H3/b15-14+/t17-,18+/m0/s1
InChI 密鑰
WWUZIQQURGPMPG-KRWOKUGFSA-N
一般說明
Highly purified preparation of bovine brain sphingosine containing >99% of the erythro isomer.
Highly purified preparation of bovine brain sphingosine containing >99% of the erythro isomer. A potent, cell-permeable, reversible, and selective inhibitor of protein kinase C (PKC; IC50 = 2.8 µM) and insulin receptor tyrosine kinase. PKC inhibition is competitive with respect to diacylglycerol, phorbol dibutyrate, and Ca2+. Does not affect the activity of myosin light chain kinase and protein kinase A. Induces apoptosis in human leukemia HL-60 cells. Note: This product is not to be used for animal treatment, in vivo research or in any other contact procedure with livestock.
生化/生理作用
Cell permeable: no
Primary Target
PKC
PKC
Product does not compete with ATP.
Reversible: no
Target IC50: 2.8 µM against PKC
警告
Toxicity: Irritant (B)
重構
Following reconstitution, aliquot, purge with N₂ gas, and freeze (-20°C). Stock solutions are stable for up to 6 months under inert atmosphere at -20°C.
法律資訊
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
危險聲明
防範說明
危險分類
Aquatic Chronic 4
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
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