860625P

C2 Dihydroceramide (d18:0/2:0)

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

• 동의어(들): N-acetoyl-D-erythro-sphinganine
• 실험식(Hill 표기법): C₂₀H₄₁NO₃
• CAS Number: 13031-64-6
• Molecular Weight: 343.54
• MDL number: MFCD00236495
• UNSPSC 코드: 12352211
• NACRES: NA.25

속성

• 양식: powder
• 포장: pkg of 1 × 5 mg (860625P-5mg)
• 제조업체/상표: Avanti Research^™ - A Croda Brand 860625P
• 지질 유형: sphingolipids
• 배송 상태: dry ice
• 저장 온도: −20°C
• SMILES string: 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
• InChI key: CRJGESKKUOMBCT-VQTJNVASSA-N

설명

일반 설명

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

애플리케이션

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.

생화학적/생리학적 작용

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.

포장

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

법적 정보

Avanti Research is a trademark of Avanti Polar Lipids, LLC

안전성 정보

• Storage Class Code: 11 - Combustible Solids