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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H22O11
Molecular Weight 342.2965
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MALTOSE ANHYDROUS

SMILES

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

InChI

InChIKey=DKXNBNKWCZZMJT-WUJBLJFYSA-N
InChI=1S/C12H22O11/c13-1-4(16)7(18)11(5(17)2-14)23-12-10(21)9(20)8(19)6(3-15)22-12/h1,4-12,14-21H,2-3H2/t4-,5+,6+,7+,8+,9-,10+,11+,12+/m0/s1

HIDE SMILES / InChI

Molecular Formula C12H22O11
Molecular Weight 342.2965
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Maltose, a disaccharide, is found mainly in grains and cereals. Nutritionally, maltose provides the same number of calories as starches and other sugars. Maltose can be the agent responsible for the primary signals to induce the sensations of hunger and satiation in human beings. It was shown, that parenterally administered maltose could be of clinical value.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Synthesis of 4'-O-acetyl-maltose and alpha-D-galactopyranosyl-(1-->4)-D-glucopyranose for biochemical studies of amylose biosynthesis.
2001 Feb 15
Sugar-pendant diamines.
2001 Jun 1
Catalytic mechanism of beta-amylase from Bacillus cereus var. mycoides: chemical rescue of hydrolytic activity for a catalytic site mutant (Glu367-->Ala) by azide.
2002 Apr
Functional characterization of the maltose ATP-binding-cassette transporter of Salmonella typhimurium by means of monoclonal antibodies directed against the MalK subunit.
2002 Aug
Structural evidence for a dominant role of nonpolar interactions in the binding of a transport/chemosensory receptor to its highly polar ligands.
2002 Jan 22
Emended descriptions of the genus Micrococcus, Micrococcus luteus (Cohn 1872) and Micrococcus lylae (Kloos et al. 1974).
2002 Mar
Comparative study of the composition of melanoidins from glucose and maltose.
2004 Jun 30
Water T2 relaxation in sugar solutions.
2005 Apr 11
A sugar's choice: coordination to a mononuclear or a dinuclear copper(II) complex?
2005 Apr 18
Selective, reversible, reagentless maltose biosensing with core-shell semiconducting nanoparticles.
2006 Feb
Direct C-glycosylation of indole with unprotected mono-, di-, and trisaccharides: a one-pot synthesis of 1-deoxy-1,1-bis(3-indolyl)alditols.
2006 Nov 27
[New look at starch degradation in Arabidopsis thaliana L. chloroplasts].
2007
The taxonomy of Enterobacter sakazakii: proposal of a new genus Cronobacter gen. nov. and descriptions of Cronobacter sakazakii comb. nov. Cronobacter sakazakii subsp. sakazakii, comb. nov., Cronobacter sakazakii subsp. malonaticus subsp. nov., Cronobacter turicensis sp. nov., Cronobacter muytjensii sp. nov., Cronobacter dublinensis sp. nov. and Cronobacter genomospecies 1.
2007 Apr 17
Effect of oxadiazolyl 3(2H)-pyridazinone on the larval growth and digestive physiology of the armyworm, Pseudaletia separata.
2008
Enhanced recombinant protein productivity by genome reduction in Bacillus subtilis.
2008 Apr 30
A comparative electron paramagnetic resonance study of the nucleotide-binding domains' catalytic cycle in the assembled maltose ATP-binding cassette importer.
2008 Sep 15
Proteome analysis of Aspergillus niger: lactate added in starch-containing medium can increase production of the mycotoxin fumonisin B2 by modifying acetyl-CoA metabolism.
2009 Dec 10
Maltose and maltodextrin utilization by Listeria monocytogenes depend on an inducible ABC transporter which is repressed by glucose.
2010 Apr 27
Isolation and characterization of lactic acid bacteria strains with ornithine producing capacity from natural sea salt.
2010 Aug
Maltose biosensing based on co-immobilization of alpha-glucosidase and pyranose oxidase.
2010 Aug
Enhancement of avermectin and ivermectin production by overexpression of the maltose ATP-binding cassette transporter in Streptomyces avermitilis.
2010 Dec
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:12:43 UTC 2023
Edited
by admin
on Fri Dec 15 15:12:43 UTC 2023
Record UNII
66Y63L379N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MALTOSE ANHYDROUS
II  
Common Name English
D-GLUCOSE, 4-O-.ALPHA.-D-GLUCOPYRANOSYL-
Systematic Name English
MALTOSE ANHYDROUS [II]
Common Name English
NSC-760396
Code English
4-O-.ALPHA.-D-GLUCOPYRANOSYL-D-GLUCOSE
Systematic Name English
D-(+)-MALTOSE
Common Name English
MALTOSE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C68472
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID1023233
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
NCI_THESAURUS
C81933
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
RXCUI
2590661
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
DAILYMED
66Y63L379N
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
PUBCHEM
181526
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
CAS
69-79-4
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
MERCK INDEX
m7048
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY Merck Index
SMS_ID
100000093003
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
CHEBI
17306
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-716-5
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
NSC
760396
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
FDA UNII
66Y63L379N
Created by admin on Fri Dec 15 15:12:43 UTC 2023 , Edited by admin on Fri Dec 15 15:12:43 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
Related Record Type Details
PARENT -> METABOLITE
Icodextrin is metabolized by alpha-amylase into oligosaccharides with a lower degree of polymerization (DP), including maltose (DP2), maltotriose (DP3), maltotetraose (DP4), and higher molecular weight species.
Related Record Type Details
ACTIVE MOIETY