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Merck
CN

860815P

Avanti

16:0(2R-OH) Ceramide

Avanti Research - A Croda Brand

别名:

N-(2′-(R)-hydroxypalmitoyl)-D-erythro-sphingosine

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关于此项目

经验公式(希尔记法):
C34H67NO4
化学文摘社编号:
分子量:
553.90
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.25
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产品名称

16:0(2R-OH) Ceramide, Avanti Research - A Croda Brand 860815P, powder

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 25 mg (860815P-25mg), pkg of 1 × 5 mg (860815P-5mg)

manufacturer/tradename

Avanti Research - A Croda Brand 860815P

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCC/C=C/[C@@H](O)[C@@H](NC([C@H](O)CCCCCCCCCCCCCC)=O)CO

InChI key

YWZGQPJRQXHVQX-GGMPIESISA-N

General description

Ceramides with 2-hydroxy fatty acids (hFA) group are present in the epidermis. 16:0(2R-OH) Ceramide is a unique ceramide containing 16C long chain base fatty acid (palmitic acid)-with 2′-hydroxyl group in R configuration.

Biochem/physiol Actions

Hydroxy fatty acid (hFA)-sphingolipids are implicated in cell signaling. They may also help in regulation of cell differentiation and apoptosis. Synthetic 2′R-hydroxy-C16-ceramide exhibits high proapoptotic activity than proapoptotic 2′S-hydroxy-C16-ceramide. hFA-ceramides in epidermis support permeability barrier function. hFA-ceramides are synthesized by fatty acid 2-hydroxylase (FA2H). Mutations of FA2H causes neurological disorders including, leukodystrophy and spastic paraparesis in humans. The mechanism of action for an antitumor drug, PM02734 involves hFA-ceramides in the cell membrane.

Packaging

5 mL Amber Glass Screw Cap Vial (860815P-25mg)
5 mL Amber Glass Screw Cap Vial (860815P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC


存储类别

11 - Combustible Solids

wgk

WGK 3



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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