MALTOTRIOSE

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 Search

SMILES

OC[C@@H](O)[C@@H](O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O)[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

Primary Target	Pharmacology	Condition	Potency
Arabidopsis chloroplast β-amylase BAM3 1 Target ID: Arabidopsis chloroplast β-amylase BAM3 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28225829	Inhibitor 8504
Pancreatic alpha-amylase 4 Target ID: CHEMBL5730 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9523717	Inhibitor 8504

PubMed

Title	Date	PubMed
Structure and hydration of the amylopectin trisaccharide building blocks--Synthesis, NMR, and molecular dynamics.	2008-12	18712853
Utilisation of pH stacking in conjunction with a highly absorbing chromophore, 5-aminofluorescein, to improve the sensitivity of capillary electrophoresis for carbohydrate analysis.	2008-07-18	18468613
DFT conformational studies of alpha-maltotriose.	2008-05	18069685
Navigation within host tissues: cues for orientation of Diplostomum spathaceum (Trematoda) in fish towards veins, head and eye.	2007-07	17316474
Direct C-glycosylation of indole with unprotected mono-, di-, and trisaccharides: a one-pot synthesis of 1-deoxy-1,1-bis(3-indolyl)alditols.	2006-11-27	16973137
Purification and biochemical characterization of an alpha-glucosidase from Xanthophyllomyces dendrorhous.	2006-01-30	16491468
Generation of furosine and color in infant/enteral formula-resembling systems.	2004-08-25	15315369
Glycopeptide-membrane interactions: glycosyl enkephalin analogues adopt turn conformations by NMR and CD in amphipathic media.	2003-05-14	12733923
Depicting the MM3 potential energy surfaces of trisaccharides by single contour maps: application to beta-cellotriose and alpha-maltotriose.	2003-01-02	12504386
pH measurements of human dental plaque after consumption of starchy foods using the microtouch and the sampling method.	1993	8242677
Maltotriose and maltotetraose excreted in urine following intravenous administration of maltose to human volunteers.	1983-07	6645121

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:51:55 GMT 2025` Edited by `admin` on `Mon Mar 31 18:51:55 GMT 2025`
Record UNII	639K0T34IK
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-170180

Preferred Name

English

MALTOTRIOSE

Common Name

English

.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-D-GLUCOPYRANOSE

Common Name

English

AMYLOTRIOSE

Common Name

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