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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H35NO15
Molecular Weight 529.4896
Optical Activity UNSPECIFIED
Defined Stereocenters 14 / 14
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of A-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]1NC(C)=O)[C@@H](O)[C@H](O)CO)O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O

InChI

InChIKey=FLZWAAFMRTZQGV-ULZIYQADSA-N
InChI=1S/C20H35NO15/c1-6-12(27)16(31)17(32)20(33-6)35-10(5-24)18(13(28)8(26)3-22)36-19-11(21-7(2)25)15(30)14(29)9(4-23)34-19/h5-6,8-20,22-23,26-32H,3-4H2,1-2H3,(H,21,25)/t6-,8+,9+,10-,11+,12+,13-,14-,15+,16+,17-,18+,19+,20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H35NO15
Molecular Weight 529.4896
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 14 / 14
E/Z Centers 0
Optical Activity UNSPECIFIED

A-TRISACCHARIDE (or Blood group A trisaccharide), a core antigen fragment in ABO blood group system. It was found to be a major urinary carbohydrate depending on diet and blood type.

Approval Year

PubMed

PubMed

TitleDatePubMed
Urinary levels of blood group A trisaccharide: observations in two siblings with neuronal ceroid lipofuscinosis.
1981 Jul 18
Conformational analysis of blood group A trisaccharide in solution and in the binding site of Dolichos biflorus lectin using transient and transferred nuclear Overhauser enhancement (NOE) and rotating-frame NOE experiments.
1996 Aug 1
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:44:32 GMT 2023
Edited
by admin
on Sat Dec 16 05:44:32 GMT 2023
Record UNII
P104QT2V1B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
A-TRISACCHARIDE
Common Name English
BG-A TRISACCHARIDE
Common Name English
BLOOD-GROUP A TRISACCHARIDE
Common Name English
ATRI
Common Name English
A TRISACCHARIDE
Common Name English
3-O-(2-ACETAMIDO-2-DEOXY-.ALPHA.-D-GALACTOPYRANOSYL)-2-O-(.ALPHA.-L-FUCOPYRANOSYL)-D-GALACTOSE
Common Name English
TRISACCHARIDE A
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 18887
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
FDA ORPHAN DRUG 20287
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
FDA ORPHAN DRUG 27988
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
FDA ORPHAN DRUG 18086
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID50198042
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
PRIMARY
PUBCHEM
71587158
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
PRIMARY
FDA UNII
P104QT2V1B
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
PRIMARY
CHEBI
35930
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
PRIMARY
CAS
49777-13-1
Created by admin on Sat Dec 16 05:44:32 GMT 2023 , Edited by admin on Sat Dec 16 05:44:32 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY