U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H32O16
Molecular Weight 504.4371
Optical Activity UNSPECIFIED
Defined Stereocenters 14 / 14
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MALTOTRIOSE

SMILES

[H][C@@](O[C@H]1O[C@H](CO)[C@@H](O[C@@]2([H])O[C@H](CO)[C@@H](O)[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=RXVWSYJTUUKTEA-CGQAXDJHSA-N
InChI=1S/C18H32O16/c19-1-5(23)9(25)15(6(24)2-20)33-18-14(30)12(28)16(8(4-22)32-18)34-17-13(29)11(27)10(26)7(3-21)31-17/h1,5-18,20-30H,2-4H2/t5-,6+,7+,8+,9+,10+,11-,12+,13+,14+,15+,16+,17+,18+/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H32O16
Molecular Weight 504.4371
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 14 / 14
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Arabidopsis chloroplast β-amylase BAM3
PubMed

PubMed

TitleDatePubMed
Maltotriose and maltotetraose excreted in urine following intravenous administration of maltose to human volunteers.
1983 Jul
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:46:04 GMT 2023
Edited
by admin
on Fri Dec 15 17:46:04 GMT 2023
Record UNII
639K0T34IK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MALTOTRIOSE
Common Name English
.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-D-GLUCOPYRANOSE
Common Name English
AMYLOTRIOSE
Common Name English
NSC-170180
Code English
GLUCOSE IMPURITY C [EP IMPURITY]
Common Name English
D-GLUCOSE, O-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-O-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-
Systematic Name English
D-MALTOTRIOSE
Common Name English
TRIOMALTOSE
Common Name English
MALTOTRIOSE [USP-RS]
Common Name English
Code System Code Type Description
RS_ITEM_NUM
1375047
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID6048963
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
PUBCHEM
92146
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
CHEBI
27931
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
CHEBI
140999
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
FDA UNII
639K0T34IK
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
CHEBI
61993
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
NSC
170180
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
WIKIPEDIA
MALTOTRIOSE
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
CAS
1109-28-0
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-174-2
Created by admin on Fri Dec 15 17:46:04 GMT 2023 , Edited by admin on Fri Dec 15 17:46:04 GMT 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.
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP