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860828P

Avanti

18:1(2S-OH) Ceramide

Avanti Polar Lipids 860828P, powder

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Synonym(s):
N-(2′-(S)-hydroxyoleoyl)-D-erythro-sphingosine
Empirical Formula (Hill Notation):
C36H69NO4
CAS Number:
Molecular Weight:
579.94
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 5 mg (860828P-5mg)

manufacturer/tradename

Avanti Polar Lipids 860828P

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)CCCCCC/C=C\CCCCCCCC)=O)CO

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18:1(2S-OH) Ceramide Avanti Polar Lipids 860828P, powder

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860828P

18:1(2S-OH) Ceramide

18:0(2S-OH) Ceramide Avanti Polar Lipids 860830P, powder

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860830P

18:0(2S-OH) Ceramide

17:0(2R-OH) Ceramide Avanti Polar Lipids 860817P, powder

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860817P

17:0(2R-OH) Ceramide

22:0(2S-OH) Ceramide Avanti Polar Lipids 860822P, powder

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860822P

22:0(2S-OH) Ceramide

packaging

pkg of 1 × 5 mg (860828P-5mg)

packaging

pkg of 1 × 5 mg (860830P-5mg)

packaging

pkg of 1 × 5 mg (860817P-5mg)

packaging

pkg of 1 × 5 mg (860822P-5mg)

manufacturer/tradename

Avanti Polar Lipids 860828P

manufacturer/tradename

Avanti Polar Lipids 860830P

manufacturer/tradename

Avanti Polar Lipids 860817P

manufacturer/tradename

Avanti Polar Lipids 860822P

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

lipid type

sphingolipids

lipid type

sphingolipids

lipid type

sphingolipids

lipid type

sphingolipids

General description

18:1(2S-OH) Ceramide is a 2S hydroxylated oleic acid-containing sphingolipid. hFA- ceramides are mainly found in epidermis.

Biochem/physiol Actions

Ceramides containing hydroxy fatty acids play a vital role in epidermal permeability barrier function.

Packaging

5 mL Amber Glass Screw Cap Vial (860828P-5mg)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Regulatory Information

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Lin Guo et al.
Journal of lipid research, 53(7), 1327-1335 (2012-04-21)
FA 2-hydroxylase (FA2H) is an NAD(P)H-dependent enzyme that initiates FA α oxidation and is also responsible for the biosynthesis of 2-hydroxy FA (2-OH FA)-containing sphingolipids in mammalian cells. The 2-OH FA is chiral due to the asymmetric carbon bearing the
Nathan L Alderson et al.
Journal of lipid research, 50(6), 1203-1208 (2009-01-28)
Sphingolipids are ubiquitous components of eukaryotic cells that regulate various cellular functions. In many cell types, a fraction of sphingolipids contain 2-hydroxy fatty acids, produced by fatty acid 2-hydroxylase (FA2H), as the N-acyl chain of ceramide [hydroxyl fatty acid (hFA)-sphingolipids].
Ana B Herrero et al.
Cancer research, 68(23), 9779-9787 (2008-12-03)
PM02734 is a novel synthetic antitumor drug that is currently in phase I clinical trials. To gain some insight into its mode of action, we used the yeast Saccharomyces cerevisiae as a model system. Treatment of S. cerevisiae with PM02734
Hiroko Hama
Biochimica et biophysica acta, 1801(4), 405-414 (2009-12-23)
2-Hydroxy fatty acids (hFA) are important components of a subset of mammalian sphingolipids. The presence of hFA in sphingolipids is best described in the nervous system, epidermis, and kidney. However, the literature also indicates that various hFA-sphingolipids are present in
Zdzislaw M Szulc et al.
Bioorganic & medicinal chemistry, 18(21), 7565-7579 (2010-09-21)
A straightforward method for the simultaneous preparation of (2S,3R,2'R)- and (2S,3R,2'S)-2'-hydroxy-ceramides (2'-OHCer) from (2S,3R)-sphingosine acetonide precursors and racemic mixtures of 2-hydroxy fatty acids (2-OHFAs) is described. The obtained 2'-OH-C4-, -C6-, -C12-, -C16-Cer and 2'-OH-C6-dhCer pairs of diastereoisomers were characterized thoroughly

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