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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
Glycopeptide-membrane interactions: glycosyl enkephalin analogues adopt turn conformations by NMR and CD in amphipathic media.
2003 May 14
DFT conformational studies of alpha-maltotriose.
2008 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:46:04 UTC 2023
Edited
by admin
on Fri Dec 15 17:46:04 UTC 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 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
EPA CompTox
DTXSID6048963
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
PUBCHEM
92146
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
CHEBI
27931
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
CHEBI
140999
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
FDA UNII
639K0T34IK
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
CHEBI
61993
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
NSC
170180
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
WIKIPEDIA
MALTOTRIOSE
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
CAS
1109-28-0
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 UTC 2023
PRIMARY
ECHA (EC/EINECS)
214-174-2
Created by admin on Fri Dec 15 17:46:04 UTC 2023 , Edited by admin on Fri Dec 15 17:46:04 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.
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP