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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H22O11
Molecular Weight 342.2965
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .BETA.-MALTOSE

SMILES

[H][C@]2(O[C@@H]1[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]1O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O

InChI

InChIKey=GUBGYTABKSRVRQ-QUYVBRFLSA-N
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

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/11246934 | https://www.ncbi.nlm.nih.gov/pubmed/28298685

Maltose, also known as maltobiose or malt sugar, is a disaccharide formed from two units of glucose joined with an α(1→4) bond, formed from a condensation reaction. Maltose was discovered by Irish chemist and brewer Cornelius O'Sullivan in 1872. Maltose is a component of malt, a substance which is obtained in the process of allowing grain to soften in water and germinate. It is found in beverages, beer, cereal, pasta, potatoes and in many processed products which have been sweetened.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
FTIR, HATR and FT-Raman studies on the anhydrous and monohydrate species of maltose in aqueous solution.
2016 Jun 16
Patents

Patents

Sample Use Guides

Anhydrous crystalline maltosewas delivered orally as a 200-mg lozenge given three times daily over a 12-week (study Alpha) or 24-week (study Omega) period to a total of 22 and 97 subjects, respectively
Route of Administration: Oral
In Vitro Use Guide
Unknown
Name Type Language
.BETA.-MALTOSE
Common Name English
MALTOSE, .BETA.-
Common Name English
.BETA.-D-GLUCOPYRANOSE, 4-O-.ALPHA.-D-GLUCOPYRANOSYL-
Systematic Name English
.BETA.-D-CELLOBIOSE
Common Name English
MALTOSE .BETA.-ANOMER
Common Name English
.BETA.-D-MALTOSE
Common Name English
Code System Code Type Description
CAS
133-99-3
Created by admin on Sat Dec 16 10:55:20 GMT 2023 , Edited by admin on Sat Dec 16 10:55:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID901318570
Created by admin on Sat Dec 16 10:55:20 GMT 2023 , Edited by admin on Sat Dec 16 10:55:20 GMT 2023
PRIMARY
PUBCHEM
6255
Created by admin on Sat Dec 16 10:55:20 GMT 2023 , Edited by admin on Sat Dec 16 10:55:20 GMT 2023
PRIMARY
FDA UNII
R4B6462NGR
Created by admin on Sat Dec 16 10:55:20 GMT 2023 , Edited by admin on Sat Dec 16 10:55:20 GMT 2023
PRIMARY