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Merck
CN

860656P

Avanti

Lyso SM (d17:1)

Avanti Research - A Croda Brand

别名:

鞘氨醇磷酸胆碱(C17碱)

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关于此项目

经验公式(希尔记法):
C22H47N2O5P
化学文摘社编号:
分子量:
450.59
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
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产品名称

Lyso SM (d17:1), Avanti Research - A Croda Brand 860656P, powder

InChI

1S/C22H47N2O5P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-22(25)21(23)20-29-30(26,27)28-19-18-24(2,3)4/h16-17,21-22,25H,5-15,18-20,23H2,1-4H3/b17-16+/t21-,22+/m0/s1

InChI key

AAERQLSYRRXFMA-FYBNUODKSA-N

SMILES string

CCCCCCCCCCCC/C=C/[C@@]([H])(O)[C@@]([H])(N)COP([O-])(OCC[N+](C)(C)C)=O

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 10 mg (860656P-10mg)
pkg of 1 × 5 mg (860656P-5mg)

manufacturer/tradename

Avanti Research - A Croda Brand 860656P

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

Biochem/physiol Actions

溶血鞘磷脂(Lyso Sm)是一种重要的脂质介质,具有调节细胞增殖、迁移、分化、代谢和凋亡的能力。它在心血管系统、免疫系统、中枢神经紧张的系统和皮肤中具有多种功能。在少数疾病状态(例如特应性皮炎,尼曼-匹克病(NPD)和癌症)中观察到Lyso SM的浓度增加。

General description

溶血鞘磷脂(Lyso SM)(d17:1)是具有长链鞘氨醇(C17碱)和亲水性磷酸胆碱的两亲性溶血磷脂Lyso SM,也称为鞘氨酰磷酸胆碱(SPC),是在血浆中发现的鞘磷脂的脱酰形式。

Packaging

5 mL棕色玻璃螺旋盖小瓶(860656P-10mg)
5 mL棕色玻璃螺旋盖小瓶(860656P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

存储类别

11 - Combustible Solids


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Di Ge et al.
Acta pharmacologica Sinica, 39(12), 1830-1836 (2018-07-28)
Sphingosylphosphorylcholine (SPC) is a bioactive sphingolipid in blood plasma that is metabolized from the hydrolysis of the membrane sphingolipid. SPC maintains low levels in the circulation under normal conditions, which makes studying its origin and action difficult. In recent years
Hong-Wei Yue et al.
International journal of clinical and experimental medicine, 8(8), 11913-11921 (2015-11-10)
Sphingosylphosphorylcholine (SPC) is a naturally occurring bioactive sphingolipid in blood plasma, metabolizing from the hydrolysis of the membrane sphingolipid. It has been shown to exert multifunctional role in cell physiological regulation either as an intracellular second messenger or as an
Wei-Lien Chuang et al.
Molecular genetics and metabolism, 111(2), 209-211 (2014-01-15)
Niemann-Pick disease type B (NPD-B) is caused by a partial deficiency of acid sphingomyelinase activity and results in the accumulation of lysosomal sphingomyelin (SPM) predominantly in macrophages. Notably, SPM is not significantly elevated in the plasma, whole blood, or urine

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