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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
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.