860468P
Avanti
N-C24:1-desoxymethylsphingosine
Avanti Research™ - A Croda Brand 860468P, powder
Synonym(e):
N-nervonoyl-1-desoxymethylsphingosine (m17:1/24:1)
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Empirische Formel (Hill-System):
C41H79NO2
CAS-Nummer:
Molekulargewicht:
618.07
MDL-Nummer:
UNSPSC-Code:
12352211
NACRES:
NA.25
Form
powder
Verpackung
pkg of 1 × 1 mg (860468P-1mg)
Hersteller/Markenname
Avanti Research™ - A Croda Brand 860468P
Lipid-Typ
bioactive lipids
sphingolipids
Versandbedingung
dry ice
Lagertemp.
−20°C
Allgemeine Beschreibung
Ceramides are generated by the acylation of the sphingoid bases, sphingosine.
Biochem./physiol. Wirkung
Deoxydihydro ceramide (deoxyDHCer), nervonoyl (C24:1) is present in the mammals along with palmitoyl (C16) dihydroceramide. In general, deoxyDHCer modulates the cellular membrane properties and may contribute to its biological functionality.
Verpackung
5 mL Amber Glass Screw Cap Vial (860468P-1mg)
Rechtliche Hinweise
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Hier finden Sie alle aktuellen Versionen:
Analysenzertifikate (COA)
Lot/Batch Number
Leider sind derzeit keine COAs für dieses Produkt online verfügbar.
Wenn Sie Hilfe benötigen, wenden Sie sich bitte an Kundensupport
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Sphingolipid biosynthesis in man and microbes
Harrison PJ, et al.
Natural Product Reports, 35(9), 921-954 (2018)
Biophysical properties of novel 1-deoxy-(dihydro) ceramides occurring in mammalian cells
Jimenez-Rojo N, et al.
Biophysical Journal, 107(12), 2850-2859 (2014)
Junliang Wan et al.
Journal of agricultural and food chemistry, 67(46), 12953-12961 (2019-10-23)
Most common sphingolipids are comprised of "typical" sphingoid bases (sphinganine, sphingosine, and structurally related compounds) and are produced via the condensation of l-serine with a fatty acyl-CoA by serine palmitoyltransferase. Some organisms, including mammals, also produce "atypical" sphingoid bases that
Sarah T Pruett et al.
Journal of lipid research, 49(8), 1621-1639 (2008-05-24)
"Sphingosin" was first described by J. L. W. Thudichum in 1884 and structurally characterized as 2S,3R,4E-2-aminooctadec-4-ene-1,3-diol in 1947 by Herb Carter, who also proposed the designation of "lipides derived from sphingosine as sphingolipides." This category of amino alcohols is now
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung.