115074-93-6

Basic information

• Product Name: soya-cerebroside II
• Synonyms: soya-cerebroside II;(2R)-N-[(1S,2R,3E,7Z)-1-(β-D-Glucopyranosyloxymethyl)-2-hydroxy-3,7-heptadecadienyl]-2-hydroxyhexadecanamide;(2S,3R,4E,8Z)-1-(β-D-Glucopyranosyloxy)-2-[[(2R)-2-hydroxypalmitoyl]amino]-4,8-octadecadiene-3-ol;(4E,8Z)-1-O-β-D-Glucopyranosyl-N-[(2R)-2-hydroxyhexadecanoyl)-4,8-sphingadienine;(R)-N-[(1S,2R,3E,7Z)-1-[(β-D-Glucopyranosyloxy)methyl]-2-hydroxy-3,7-heptadecadienyl]-2-hydroxyhexadecanamide;Cerebroside B1b
• CAS NO: 115074-93-6
• Molecular Formula: C₄₀H₇₅NO₉
• Molecular Weight: 714.02
• Mol File: 115074-93-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 192-194 °C
• Boiling Point: 870.1°Cat760mmHg
• Flash Point: 480°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 2.41E-35mmHg at 25°C
• Refractive Index: 1.529
• PKA: 12.89±0.70(Predicted)
• CAS DataBase Reference: soya-cerebroside II(CAS DataBase Reference)
• NIST Chemistry Reference: soya-cerebroside II(115074-93-6)
• EPA Substance Registry System: soya-cerebroside II(115074-93-6)

Safety Data

• Hazardous Substances Data: 115074-93-6(Hazardous Substances Data)

Usage

General Description

Soya-cerebroside II is a chemical compound derived from soybeans. It's a type of sphingolipid, a class of lipids known for their role in cell structure and signaling. This molecule has been studied for its potential benefits to human health, such as anti-inflammatory and anti-cancer properties. In addition, research indicates that soya-cerebroside II may help regulate lipid metabolism, potentially offering protection against conditions like atherosclerosis and obesity. However, more research is needed to fully understand its functions and potential applications in medicine and health.

InChI:InChI=1/C40H75NO9/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-33(43)32(31-49-40-38(47)37(46)36(45)35(30-42)50-40)41-39(48)34(44)29-27-25-23-21-18-16-14-12-10-8-6-4-2/h19-20,26,28,32-38,40,42-47H,3-18,21-25,27,29-31H2,1-2H3,(H,41,48)/b20-19-,28-26+/t32?,33-,34-,35-,36-,37+,38-,40+/m1/s1

Upstream product

• 88195-82-8 p-nitrophenyl 2-O-acetyl-(2R)-2-hydroxypalmitate 
• 95603-89-7 D(R)-α-acetoxypalmitic acid 
• 77295-69-3 1,1-dibromo-1-undecene 
• 74808-10-9 O-(2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl)trichloroacetimidate 
• 16742-51-1 methyl 2-hydroxypalmitate 
• 112-39-0 hexadecanoic acid methyl ester 
• 16452-51-0 (R)-(-)-2-hydroxyhexadecanoic acid 
• 112-31-2 caprinaldehyde 
• 262593-01-1 Acetic acid (2E,6Z)-(R)-1-[(S)-1-((R)-2-acetoxy-hexadecanoylamino)-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-hexadeca-2,6-dienyl ester 
• 262593-00-0 (2S,3R,4E,8Z,2'R)-1-(t-butyldiphenylsilyl)oxy-2-(2'-hydroxyhexadecanoyl)amino-4,8-octadien-3-ol 
• 262593-02-2 (2S,3R,4E,8Z,2'R)-3-acetoxy-2-(2'-acetoxyhexadecanoyl)amino-4,8-octadien-1-ol 
• 262592-93-8 (1R,2E,4'S)-5-cyano-1-(2'-phenyl-4',5'-dihydrooxazol-4'-yl)-2-penten-1-ol 
• 262592-87-0 (1R,2E,4'S)-1-(2'-phenyl-4',5'-dihdyrooxazol-4'-yl)hepta-2,6-dien-1-ol 
• 262592-94-9 (1R,2E,4'S)-5-formyl-1-(2'-phenyl-4',5'-dihydrooxazol-4'-yl)-2-penten-1-ol 

Downstream Products

• 16742-51-1 methyl 2-hydroxypalmitate 
• 25277-68-3 (4E,8E)-2-Amino-octadeca-4,8-diene-1,3-diol 
• 114200-59-8 (2R,3R,4S,5S,6R)-2-((4E,8E)-2-Amino-3-hydroxy-octadeca-4,8-dienyloxy)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 
• 13552-09-5 2-aminooctadecan-1,3-diol 

Relevant articles and documents

Synthesis of sphingadienine-type glucocerebrosides

Sphinga-4,8-dienine derivatives were synthesized from a vinyl-epoxide 5 via three routes. First, reaction of 5 with 2-dodecenyl cyanocuprate afforded a 1:1 mixture of (4E,8E)- and (4E,8Z)-sphingadienine derivatives in high yield. Second, the (4E,8E)-isome

Synthesis of cerebroside B(1b) with antiulcerogenic activity II(1)). Total synthesis and determination of absolute configuration of cerebroside B(1b) and its stereoisomers

-

Total synthesis and determination of absolute configuration of cererboside B(1b) and its stereoisomers

-