U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H32O15
Molecular Weight 488.4377
Optical Activity UNSPECIFIED
Defined Stereocenters 14 / 14
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of B-TRISACCHARIDE

SMILES

[H][C@@]2(O[C@@H](C=O)[C@@H](O[C@@]1([H])O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@@H](O)[C@H](O)CO)O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O

InChI

InChIKey=OZIOWHWTZWIMCZ-MPUPURDASA-N
InChI=1S/C18H32O15/c1-5-9(23)12(26)14(28)17(30-5)32-8(4-21)16(10(24)6(22)2-19)33-18-15(29)13(27)11(25)7(3-20)31-18/h4-20,22-29H,2-3H2,1H3/t5-,6+,7+,8-,9+,10-,11-,12+,13-,14-,15+,16+,17-,18+/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H32O15
Molecular Weight 488.4377
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 14 / 14
E/Z Centers 0
Optical Activity UNSPECIFIED

B-Trisaccharide belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. B-Trisaccharide in blood group B is excreted when an individual is given Galactose. The B-trisaccharide was the only oligosaccharide detected in plasma after galactose administration to a blood-group-B secretor individual. The structure of the branched blood group B trisaccharide alone has been studied both by X-ray crystallography and by NMR.

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 07:03:09 GMT 2023
Edited
by admin
on Sat Dec 16 07:03:09 GMT 2023
Record UNII
2P888H42QS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
B-TRISACCHARIDE
Common Name English
TRISACCHARIDE B
Common Name English
.ALPHA.-D-GAL-(1->3)-(.ALPHA.-L-FUC-(1->2))-D-GAL
Common Name English
BLOOD GROUP B TRISACCHARIDE
Common Name English
3-O-(.ALPHA.-D-GALACTOPYRANOSYL)-2-O-(.ALPHA.-L-FUCOPYRANOSYL)-D-GALACTOSE
Common Name English
B TRISACCHARIDE
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 27988
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
FDA ORPHAN DRUG 18887
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
FDA ORPHAN DRUG 18086
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
FDA ORPHAN DRUG 20287
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
Code System Code Type Description
CAS
49777-14-2
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
PRIMARY
FDA UNII
2P888H42QS
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
PRIMARY
CHEBI
61010
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID001045087
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
PRIMARY
PUBCHEM
54177368
Created by admin on Sat Dec 16 07:03:09 GMT 2023 , Edited by admin on Sat Dec 16 07:03:09 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY