Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:60167 - α-
D
-
Gal-
(1→6)-
α-
D
-
Gal-
(1→6)-
β-
D
-
Glc-
(1↔2)-
Fru
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
α-
D
-
Gal-
(1→6)-
α-
D
-
Gal-
(1→6)-
β-
D
-
Glc-
(1↔2)-
Fru
ChEBI ID
CHEBI:60167
ChEBI ASCII Name
alpha-D-Gal-(1->6)-alpha-D-Gal-(1->6)-beta-D-Glc-(1<->2)-Fru
Definition
A tetrasaccharide with no free anomeric centre consisting of two galactosyl residues, one glucosyl residue and one fructosyl residue in a liner sequence, linked as shown.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C24H42O21
Net Charge
0
Average Mass
666.579
Monoisotopic Mass
666.22186
InChI
InChI=1S/C24H42O21/c25-
1-
6-
10(28)
14(32)
17(35)
21(41-
6)
39-
3-
8-
11(29)
15(33)
18(36)
22(42-
8)
40-
4-
9-
12(30)
16(34)
19(37)
23(43-
9)
45-
24(5-
27)
20(38)
13(31)
7(2-
26)
44-
24/h6-
23,25-
38H,1-
5H2/t6-
,7-
,8-
,9-
,10+,11+,12-
,13-
,14+,15+,16+,17-
,18-
,19-
,20+,21+,22+,23+,24?/m1/s1
InChIKey
UQZIYBXSHAGNOE-GDNDFQKDSA-N
SMILES
OC[C@H]
1OC(CO)
(O[C@@H]
2O[C@H]
(CO[C@H]
3O[C@H]
(CO[C@H]
4O[C@H]
(CO)
[C@H]
(O)
[C@H]
(O)
[C@H]
4O)
[C@H]
(O)
[C@H]
(O)
[C@H]
3O)
[C@@H]
(O)
[C@H]
(O)
[C@H]
2O)
[C@@H]
(O)
[C@@H]
1O
ChEBI Ontology
Outgoing
α-
D
-
Gal-
(1→6)-
α-
D
-
Gal-
(1→6)-
β-
D
-
Glc-
(1↔2)-
Fru (
CHEBI:60167
)
is a
tetrasaccharide (
CHEBI:50126
)
IUPAC Name
D
-
fructofuranosyl α-
D
-
galactopyranosyl-
(1→6)-
α-
D
-
galactopyranosyl-
(1→6)-
β-
D
-
glucopyranoside
Synonym
Source
α-
D
-
Gal
p
-
(1→6)-
α-
D
-
Gal
p
-
(1→6)-
β-
D
-
Glc
p
-
(1↔2)-
Fru
f
ChEBI
Registry Number
Type
Source
46878592
Reaxys Registry Number
Reaxys
Citation
Type
Source
19913595
PubMed citation
Europe PMC
Last Modified
20 January 2022