- 商品介绍
- 规格参数
- 包装参数
General description
Contains primarily nervonic and stearic acids. Precursor to ceramide second messengers via the action of sphingomyelinase.
Contains primarily stearic and nervonic acids. Generates ceramide, a second messenger via the action of sphingomyelinase. Zwitterionic at pH 7.0.
Note: This product is not to be used for animal treatment, in vivo research or in any other contact procedure with livestock.
Biochem/physiol Actions
Cell permeable: no
Primary Target
Precursor to ceramide second messengers via the action of sphingomyelinase.
Product does not compete with ATP.
Reversible: no
Preparation Note
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Other Notes
Tonetti, M., et al. 1998. Biochimie 80, 923.
Naundorf, A. and Klaffke, W. 1996. Carbohydr. Res. 285, 141.
Slife, C.W., et al. 1989. J. Biol. Chem.264, 10371.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
| Quality Segment | 100 |
| description | Merck USA index - 14, 8746 |
| assay | ≥98% (TLC) |
| form | solid |
| manufacturer/tradename | Calbiochem® |
| storage condition | OK to freeze |
| color | white |
| solubility | ethanol: 1 mg/mL,acetic acid: 5 mg/mL,chloroform: 5 mg/mL |
| shipped in | ambient |
| storage temp. | −20°C |
| SMILES string | [P](=O)(OC[C@H](NC=O)[C@H](O)\C=C\CCCCCCCCCCCCC)(OCC[N+](C)(C)C)O |
| InChI | 1S/C24H49N2O6P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-24(28)23(25-22-27)21-32-33(29,30)31-20-19-26(2,3)4/h17-18,22-24,28H,5-16,19-21H2,1-4H3,(H-,25,27,29,30)/p+1/b18-17+/t23-,24+/m0/s1 |
| InChI key | LRYZPFWEZHSTHD-HEFFAWAOSA-O |
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¥ 2814.26
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¥ 1779.22
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¥ 4173.75
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¥ 8982.64
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¥ 2666.57
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¥ 1156.91
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¥ 3852.13
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¥ 3662.39
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¥ 2754.43
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