MiMeDB: Showing metabocard for alpha-maltose (MMDBc0054340)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-05 23:07:51 UTC

Update Date

2022-09-01 02:28:34 UTC

Metabolite ID

MMDBc0054340

Metabolite Identification

Common Name

alpha-maltose

Description

Nonsweet nutritive food additive used as a reduced calorie fat replacement. Also used as a stabiliser, thickener and encapsulating agent in food products.Maltodextrin is a polysaccharide that is used as a food additive. It is hydrolysate produced from starch and is usually found as a creamy-white hygroscopic spraydried powder. Maltodextrin is easily digestible, being absorbed as rapidly as glucose, and might be either moderately sweet or almost flavorless.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
4-O-alpha-D-Glucopyranosyl-alpha-D-glucopyranose	ChEBI
alpha-D-GLCP-(1->4)-alpha-D-GLCP	ChEBI
alpha-Malt sugar	ChEBI
Glca1-4glca	ChEBI
Glcalpha1-4glca	ChEBI
Glcalpha1-4glcalpha	ChEBI
MALTOSE	ChEBI
4-O-a-D-Glucopyranosyl-a-D-glucopyranose	Generator
4-O-Α-D-glucopyranosyl-α-D-glucopyranose	Generator
a-D-GLCP-(1->4)-a-D-GLCP	Generator
Α-D-GLCP-(1->4)-α-D-GLCP	Generator
a-Malt sugar	Generator
Α-malt sugar	Generator
a-Maltose	Generator, HMDB
α-maltose	Generator, HMDB
Linear maltodextrin	HMDB
Maltodextrin(N)	HMDB
Maltodextrin(N-2)	HMDB

Molecular Formula

(C₁₂H₂₂O₁₁)n

Average Mass

Not Available

Monoisotopic Mass

Not Available

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

Not Available

InChI Identifier

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

InChI Key

GUBGYTABKSRVRQ-ASMJPISFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Disaccharide
Oxane
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

maltose (CHEBI:18167 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Not Available

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Firmicutes	1	Human feces

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0037138

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB016133

KNApSAcK ID

Not Available

Chemspider ID

388469

KEGG Compound ID

C00897

BioCyc ID

ALPHA-MALTOSE

BiGG ID

Not Available

Wikipedia Link

Maltose

METLIN ID

Not Available

PubChem Compound

439341

PDB ID

Not Available

ChEBI ID

18167

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]
Yannai, Shmuel (2004). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. Boca Raton: Chapman & Hall/CRC..

Showing metabocard for alpha-maltose (MMDBc0054340)

MOL for #<Metabolite:0x0000560be2976820>

3D MOL for #<Metabolite:0x0000560be2976820>

3D SDF for #<Metabolite:0x0000560be2976820>

3D-SDF for #<Metabolite:0x0000560be2976820>

PDB for #<Metabolite:0x0000560be2976820>

3D PDB for #<Metabolite:0x0000560be2976820>

SMILES for #<Metabolite:0x0000560be2976820>

INCHI for #<Metabolite:0x0000560be2976820>

Structure for #<Metabolite:0x0000560be2976820>

3D Structure for #<Metabolite:0x0000560be2976820>