Top Suppliers:I want be here



114297-20-0

114297-20-0 structure
114297-20-0 structure
  • Name: Soyacerebroside I
  • Chemical Name: (2R)-2-hydroxy-N-[(3R,4E,8E)-3-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]hexadecanamide
  • CAS Number: 114297-20-0
  • Molecular Formula: C40H75NO9
  • Molecular Weight: 714.02
  • Catalog: Research Areas Others
  • Create Date: 2017-06-22 20:01:02
  • Modify Date: 2025-08-23 22:54:12
  • Soyacerebroside I is a glycosphingolipid, together with Soyacerebroside II, which can be isolated from the seeds of Glycine max Merrill (Leguminosae). Soyacerebroside II shows ionophoretic activity for Ca2+[1].

Name (2R)-2-hydroxy-N-[(3R,4E,8E)-3-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]hexadecanamide
Synonyms (2R)-N-[(2S,3R,4E,8E)-1-(β-D-Glucopyranosyloxy)-3-hydroxy-4,8-octadecadien-2-yl]-2-hydroxyhexadecanamide
Hexadecanamide, N-[(1S,2R,3E,7E)-1-[(β-D-glucopyranosyloxy)methyl]-2-hydroxy-3,7-heptadecadien-1-yl]-2-hydroxy-, (2R)-
Soya-cerebroside I
Description Soyacerebroside I is a glycosphingolipid, together with Soyacerebroside II, which can be isolated from the seeds of Glycine max Merrill (Leguminosae). Soyacerebroside II shows ionophoretic activity for Ca2+[1].
Related Catalog
References

[1]. Shibuya H, et al. Sphingolipids and glycerolipids. I. Chemical structures and ionophoretic activities of soya-cerebrosides I and II from soybean. Chem Pharm Bull (Tokyo). 1990 Nov;38(11):2933-8.  

Density 1.1±0.1 g/cm3
Boiling Point 870.1±65.0 °C at 760 mmHg
Molecular Formula C40H75NO9
Molecular Weight 714.02
Flash Point 480.0±34.3 °C
Exact Mass 713.544189
PSA 168.94000
LogP 10.07
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.530
Hazard Codes Xi
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.