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860025P

Avanti

Brain Sphingosine

D-erythro-Sphingosine (Brain, Porcine), powder

同義詞:

Sphingosine 2S, 3R; D-erythro-Sphingosine; (2S,3R,4E)-2-aminooctadec-4-ene-1,3-diol; (2S,3R,4E)-2-amino-1,3-octadec-4-enediol

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About This Item

CAS號碼:
分類程式碼代碼:
12352211
NACRES:
NA.25

化驗

>99% (TLC)

形狀

powder

包裝

pkg of 1 × 5 mg (860025P-5mg)

製造商/商標名

Avanti Research - A Croda Brand 860025P

脂質類型

sphingolipids

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

OC[C@@](N)([H])[C@]([H])(O)/C=C/CCCCCCCCCCCCC

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

Brain sphingosine is a central metabolite, which is produced from the de novo synthesis of cellular sphingolipids. It is involved in growth, differentiation, survival and cell death. D-erythro-Sphingosine acts as a pharmacological inhibitor of protein kinase C in human platelets. It prevents platelet aggregation in cells.

應用

Brain sphingosine has been used as a standard in the fluorimetric determination of sphingosine in porcine enterocyte monosialogangliosides.

包裝

5 mL Amber Glass Screw Cap Vial (860025P-5mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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M D Rolsma et al.
Journal of virology, 72(11), 9079-9091 (1998-10-10)
A ganglioside fraction isolated from pooled intestines from newborn to 4-week-old piglets, which we previously partially characterized and showed to specifically inhibit the binding of porcine rotavirus (OSU strain) to host cells (M. D. Rolsma, H. B. Gelberg, and M.
Structure and function of a ganglioside receptor for porcine rotavirus
Rolsma MD, et al.
Journal of Virology, 72(11), 9079-9091 (1998)
Use of D-erythro-sphingosine as a pharmacological inhibitor of protein kinase C in human platelets
Khan WA, et al.
The Biochemical Journal, 278(2), 387-392 (1991)
Activation of the melastatin-related cation channel TRPM3 by D-erythro-sphingosine
Grimm C, et al.
Molecular Pharmacology, 67(3), 798-805 (2005)

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