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InChI=1S/CH4O/c1-2/h2H,1H3
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> Main
CHEBI:18167 - α-maltose
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ChEBI Name
α-maltose
ChEBI ID
CHEBI:18167
ChEBI ASCII Name
alpha-maltose
Definition
A maltose that has α-configuration at the reducing end anomeric centre.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:43893, CHEBI:10300, CHEBI:12340, CHEBI:22463
Supplier Information
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Read full article at Wikipedia
Formula
C12H22O11
Net Charge
0
Average Mass
342.29648
Monoisotopic Mass
342.11621
InChI
InChI=1S/C12H22O11/c13-
1-
3-
5(15)
6(16)
9(19)
12(22-
3)
23-
10-
4(2-
14)
21-
11(20)
8(18)
7(10)
17/h3-
20H,1-
2H2/t3-
,4-
,5-
,6+,7-
,8-
,9-
,10-
,11+,12-
/m1/s1
InChIKey
GUBGYTABKSRVRQ-ASMJPISFSA-N
SMILES
OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
Roles Classification
Biological Role
(s):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
(via
maltose
)
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
(via
maltose
)
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
(via
maltose
)
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
(via
maltose
)
sweetening agent
Substance that sweeten food, beverages, medications, etc.
(via
maltose
)
Application
(s):
sweetening agent
Substance that sweeten food, beverages, medications, etc.
(via
maltose
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
α-maltose (
CHEBI:18167
)
is a
maltose (
CHEBI:17306
)
Incoming
α-
D
-Glc
p
-(1→3)-[α-
D
-Glc
p
-(1→4)]-α-
D
-Glc
p
(
CHEBI:148042
)
has functional parent
α-maltose (
CHEBI:18167
)
α-
D
-Glc
p
-(1→4)-α-
D
-Glc
p
-(1→3)-
D
-Glc
p
(
CHEBI:146798
)
has functional parent
α-maltose (
CHEBI:18167
)
1-
O
-acetyl-α-maltose (
CHEBI:2411
)
has functional parent
α-maltose (
CHEBI:18167
)
IUPAC Name
α-
D
-glucopyranosyl-(1→4)-α-
D
-glucopyranose
Synonyms
Sources
4-O-alpha-D-glucopyranosyl-alpha-D-glucopyranose
PDBeChem
4-
O
-α-
D
-glucopyranosyl-α-
D
-glucopyranose
IUPAC
α-
D
-Glc
p
-(1→4)-α-
D
-Glc
p
IUPAC
alpha-Malt sugar
KEGG COMPOUND
alpha-Maltose
KEGG COMPOUND
α-maltose
UniProt
Glca1-4Glca
ChEBI
Glcα1-4Glca
ChEBI
Glcα1-4Glcα
ChEBI
MALTOSE
PDBeChem
Manual Xrefs
Databases
ALPHA-MALTOSE
MetaCyc
C00897
KEGG COMPOUND
HMDB0000163
HMDB
MAL
PDBeChem
Maltose
Wikipedia
View more database links
Registry Numbers
Types
Sources
1292753
Reaxys Registry Number
Reaxys
1292753
Beilstein Registry Number
Beilstein
1485260
Gmelin Registry Number
Gmelin
4482-75-1
CAS Registry Number
KEGG COMPOUND
Citations
Types
Sources
17669381
PubMed citation
Europe PMC
19443021
PubMed citation
Europe PMC
25568069
PubMed citation
Europe PMC
31537530
PubMed citation
Europe PMC
Last Modified
11 May 2020