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Merck
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Key Documents

567726

Sigma-Aldrich

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

经验公式(希尔记法):
C18H37NO2
CAS号:
分子量:
299.49
MDL號碼:
分類程式碼代碼:
12352211
NACRES:
NA.77

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
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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