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> Main
CHEBI:18147 - β-maltose
Main
ChEBI Ontology
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ChEBI Name
β-maltose
ChEBI ID
CHEBI:18147
ChEBI ASCII Name
beta-maltose
Definition
A maltose that has β-configuration at the reducing end anomeric centre.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:10431, CHEBI:12396, CHEBI:22848
Supplier Information
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Wikipedia
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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-QUYVBRFLSA-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):
geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
sweetening agent
Substance that sweeten food, beverages, medications, etc.
(via
maltose
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
β-maltose (
CHEBI:18147
)
has role
geroprotector (
CHEBI:176497
)
β-maltose (
CHEBI:18147
)
is a
maltose (
CHEBI:17306
)
Incoming
α-
D
-Glc
p
-(1→4)-β-
D
-Glc
p
-(1→6)-β-
D
-Glc
p
(
CHEBI:148799
)
has functional parent
β-maltose (
CHEBI:18147
)
α-
D
-Glc
p
-(1→4)-[α-
D
-Glc
p
-(1→6)]-β-
D
-Glc
p
(
CHEBI:147798
)
has functional parent
β-maltose (
CHEBI:18147
)
α-
D
-Glc
p
-(1→4)-[β-
D
-Glc
p
-(1→6)]-β-
D
-Glc
p
(
CHEBI:146926
)
has functional parent
β-maltose (
CHEBI:18147
)
1-
O
-acetyl-β-maltose (
CHEBI:15352
)
has functional parent
β-maltose (
CHEBI:18147
)
decyl β-
D
-maltopyranoside (
CHEBI:67097
)
has functional parent
β-maltose (
CHEBI:18147
)
dodecyl β-
D
-maltoside (
CHEBI:43769
)
has parent hydride
β-maltose (
CHEBI:18147
)
IUPAC Name
α-
D
-glucopyranosyl-(1→4)-β-
D
-glucopyranose
Synonyms
Sources
4-(alpha-D-Glucopyranosido)-alpha-glucopyranose
ChemIDplus
4-
O
-α-
D
-glucopyranosyl-β-
D
-glucopyranose
IUPAC
4-O-alpha-D-Glucopyranosyl-D-glucose
ChemIDplus
α-
D
-Glc
p
-(1→4)-β-
D
-Glc
p
IUPAC
β-
D
-glucopyranose, 4-
O
-α-
D
-glucopyranosyl-
ChEBI
beta-Maltose
KEGG COMPOUND
β-maltose
UniProt
D-Maltose
ChemIDplus
Glca1-4Glcb
ChEBI
Glcα1-4Glcβ
ChEBI
Maltobiose
ChemIDplus
Manual Xrefs
Databases
1628
DrugCentral
C01971
KEGG COMPOUND
CN101484460
Patent
EP2045255
Patent
KR20090026341
Patent
Maltose
Wikipedia
MALTOSE
MetaCyc
US2009292116
Patent
View more database links
Registry Numbers
Types
Sources
133-99-3
CAS Registry Number
KEGG COMPOUND
1617409
Gmelin Registry Number
Gmelin
5758727
Beilstein Registry Number
Beilstein
69-79-4
CAS Registry Number
ChemIDplus
90844
Reaxys Registry Number
Reaxys
Citations
Types
Sources
10923783
PubMed citation
Europe PMC
15665241
PubMed citation
Europe PMC
17439666
PubMed citation
Europe PMC
1839610
PubMed citation
Europe PMC
19443021
PubMed citation
Europe PMC
20477758
PubMed citation
Europe PMC
20480118
PubMed citation
Europe PMC
31537530
PubMed citation
Europe PMC
7796915
PubMed citation
Europe PMC
8495446
PubMed citation
Europe PMC
Last Modified
25 June 2024