860625P

C2 Dihydroceramide (d18:0/2:0)

Avanti Research^™ - A Croda Brand 860625P, powder

• Synonyme(s) : N-acetoyl-D-erythro-sphinganine
• Formule empirique (notation de Hill) : C₂₀H₄₁NO₃
• CAS Number: 13031-64-6
• Poids moléculaire : 343.54
• Numéro MDL: MFCD00236495
• Code UNSPSC : 12352211
• Nomenclature NACRES : NA.25

Propriétés

• Forme: powder
• Conditionnement: pkg of 1 × 5 mg (860625P-5mg)
• Fabricant/nom de marque: Avanti Research^™ - A Croda Brand 860625P
• Type de lipide: sphingolipids
• Conditions d'expédition: dry ice
• Température de stockage: −20°C
• Chaîne SMILES: OC[C@]([H])(NC(C)=O)[C@]([H])(O)CCCCCCCCCCCCCCC
• InChI: 1S/C20H41NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20(24)19(17-22)21-18(2)23/h19-20,22,24H,3-17H2,1-2H3,(H,21,23)/t19-,20+/m0/s1
• Clé InChI: CRJGESKKUOMBCT-VQTJNVASSA-N

Description

Description générale

Dihydroceramide belongs to the ceramide family. It contains sphinganine, which is devoid of the 4,5-trans-double bond in the sphingoid base backbone.

Application

C2 Dihydroceramide (d18:0/2:0) has been used as a lipid standard in the analysis of sphingolipids by tandem mass spectrometry. It is also suitable for inducing stress in embryos to study stress-induced apoptosis in larval embryos of Japanese flounder.

Actions biochimiques/physiologiques

Dihydroceramide is synthesized by the N-acylation of dihydrosphingosine. It functions as an inactive precursor for ceramide in de novo sphingolipid synthesis. (Dihydro)-ceramide desaturase catalyzes the conversion of dihydroceramide to ceramide by the addition of C4−5 trans-double bond in the sphingoid backbone. Dihydroceramide has an ability to induce autophagy.

Conditionnement

5 mL Amber Glass Screw Cap Vial (860625P-5mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids