CHEBI:18147 - β-maltose

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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
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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): sweetening agent
Substance that sweeten food, beverages, medications, etc.
(via maltose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-maltose (CHEBI:18147) is a maltose (CHEBI:17306)
Incoming 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-Glcp-(1→4)-β-D-Glcp IUPAC
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
90844 Beilstein Registry Number Beilstein
Citations Waiting for 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
20480118 PubMed citation Europe PMC
7796915 PubMed citation Europe PMC
8495446 PubMed citation Europe PMC
Last Modified
22 February 2017