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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H42O21
Molecular Weight 666.5777
Optical Activity UNSPECIFIED
Defined Stereocenters 19 / 19
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MALTOTETRAOSE

SMILES

[H][C@@](O[C@H]1O[C@H](CO)[C@@]([H])(O[C@H]2O[C@H](CO)[C@@H](O[C@@]3([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)([C@H](O)CO)[C@H](O)[C@@H](O)C=O

InChI

InChIKey=UYQJCPNSAVWAFU-KVXMBEGHSA-N
InChI=1S/C24H42O21/c25-1-6(30)11(32)19(7(31)2-26)43-23-17(38)14(35)21(9(4-28)41-23)45-24-18(39)15(36)20(10(5-29)42-24)44-22-16(37)13(34)12(33)8(3-27)40-22/h1,6-24,26-39H,2-5H2/t6-,7+,8+,9+,10+,11+,12+,13-,14+,15+,16+,17+,18+,19+,20+,21+,22+,23+,24+/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H42O21
Molecular Weight 666.5777
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 19 / 19
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Generation of furosine and color in infant/enteral formula-resembling systems.
2004 Aug 25
DFT conformation and energies of amylose fragments at atomic resolution. Part 2: 'Band-flip' and 'kink' forms of alpha-maltotetraose.
2009 Feb 17
DFT conformation and energies of amylose fragments at atomic resolution. Part 1: Syn forms of alpha-maltotetraose.
2009 Feb 17
Characterization of nimbidiol as a potent intestinal disaccharidase and glucoamylase inhibitor present in Azadirachta indica (neem) useful for the treatment of diabetes.
2013 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:50:29 UTC 2023
Edited
by admin
on Fri Dec 15 17:50:29 UTC 2023
Record UNII
BO88JLT87R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MALTOTETRAOSE
Common Name English
.ALPHA.-1,4-TETRAGLUCOSE
Common Name English
AMYLOTETRAOSE
Common Name English
D-GLUCOSE, O-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-O-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-O-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID50865722
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
CAS
34612-38-9
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
CHEBI
143180
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
CHEBI
28460
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
DRUG BANK
DB02237
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
CHEBI
61988
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
FDA UNII
BO88JLT87R
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
PUBCHEM
123966
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
ECHA (EC/EINECS)
252-111-0
Created by admin on Fri Dec 15 17:50:29 UTC 2023 , Edited by admin on Fri Dec 15 17:50:29 UTC 2023
PRIMARY
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.