CHEBI:17306 - maltose

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ChEBI Name maltose ChEBI ID CHEBI:17306 Definition A glycosylglucose consisting of two D-glucopyranose units connected by an α-(1→4)-linkage. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:6668, CHEBI:14568, CHEBI:25144 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License 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-PICCSMPSSA-N SMILES OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)OC(O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed Escherichia coli (NCBI:txid562) See: PubMed Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). sweetening agent Substance that sweeten food, beverages, medications, etc. Application(s): sweetening agent Substance that sweeten food, beverages, medications, etc. View more via ChEBI Ontology ChEBI Ontology Outgoing maltose (CHEBI:17306) has role Escherichia coli metabolite (CHEBI:76971) maltose (CHEBI:17306) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) maltose (CHEBI:17306) has role human metabolite (CHEBI:77746) maltose (CHEBI:17306) has role mouse metabolite (CHEBI:75771) maltose (CHEBI:17306) has role sweetening agent (CHEBI:50505) maltose (CHEBI:17306) is a glycosylglucose (CHEBI:24405) maltose (CHEBI:17306) is a maltooligosaccharide (CHEBI:17593) Incoming α-D-Glcp-(1→3)-[α-D-Glcp-(1→4)]-D-Glcp (CHEBI:148380) has functional parent maltose (CHEBI:17306) α-D-Glcp-(1→4)-[α-D-Glcp-(1→6)]-D-Glcp (CHEBI:147961) has functional parent maltose (CHEBI:17306) α-D-Glcp-(1→4)-[β-D-Glcp-(1→2)]-D-Glcp (CHEBI:148586) has functional parent maltose (CHEBI:17306) α-maltose 6'-phosphate (CHEBI:15703) has functional parent maltose (CHEBI:17306) β-D-Galp-(1→4)-α-D-Glcp-(1→4)-D-Glcp (CHEBI:149416) has functional parent maltose (CHEBI:17306) β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-D-Glcp (CHEBI:149222) has functional parent maltose (CHEBI:17306) 1-O-acetylmaltose (CHEBI:13714) has functional parent maltose (CHEBI:17306) maltose phosphate (CHEBI:25143) has functional parent maltose (CHEBI:17306) royal jelly (CHEBI:78665) has part maltose (CHEBI:17306) α-maltose (CHEBI:18167) is a maltose (CHEBI:17306) β-maltose (CHEBI:18147) is a maltose (CHEBI:17306) IUPAC Names α-D-glucopyranosyl-(1→4)-D-glucopyranose α-D-glucopyranosyl-(1→4)-D-glucose Synonyms Sources 1-alpha-D-Glucopyranosyl-4-alpha-D-glucopyranose KEGG COMPOUND 4-(α-D-glucopyranosido)-α-glucopyranose NIST Chemistry WebBook 4-(α-D-glucosido)-D-glucose NIST Chemistry WebBook 4-O-α-D-glucopyranosyl-D-glucopyranose IUPAC 4-O-α-D-glucopyranosyl-D-glucose NIST Chemistry WebBook α-D-Glcp-(1→4)-D-Glcp IUPAC alpha-D-Glucopyranosyl-(1->4)-D-glucopyranose KEGG COMPOUND α-malt sugar NIST Chemistry WebBook Cextromaltose NIST Chemistry WebBook D-(+)-maltose ChemIDplus D-maltose UniProt D-maltose NIST Chemistry WebBook Malt sugar KEGG COMPOUND maltobiose NIST Chemistry WebBook Maltose KEGG COMPOUND Malzzucker ChEBI Manual Xrefs Databases C00001140 KNApSAcK C00208 KEGG COMPOUND D00044 KEGG DRUG DB03323 DrugBank G00275 KEGG GLYCAN Maltose Wikipedia View more database links Registry Numbers Types Sources 1292747 Reaxys Registry Number Reaxys 1292747 Beilstein Registry Number Beilstein 69-79-4 CAS Registry Number ChemIDplus 69-79-4 CAS Registry Number NIST Chemistry WebBook Citations Types Sources 16332759 PubMed citation Europe PMC 17723085 PubMed citation Europe PMC 22094343 PubMed citation Europe PMC 22185612 PubMed citation Europe PMC 22246222 PubMed citation Europe PMC 22252265 PubMed citation Europe PMC 22411612 PubMed citation Europe PMC 22424089 PubMed citation Europe PMC 22451670 PubMed citation Europe PMC 22469630 PubMed citation Europe PMC 22529943 PubMed citation Europe PMC 22573161 PubMed citation Europe PMC 22669197 PubMed citation Europe PMC Last Modified 23 May 2020