Page last updated: 2024-11-06

isomaltulose

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

6-O-alpha-D-glucopyranosyl-D-fructofuranose : A glycosylfructose that is D-fructofuranose attached to a alpha-D-glucopyranosyl unit at position 6 via a glycosidic linkage. It is found in honey and sugarcane. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID439559
CHEBI ID18394
SCHEMBL ID118910
MeSH IDM0051828

Synonyms (16)

Synonym
CHEBI:18394
6-o-alpha-d-glucopyranosyl-d-fructofuranose
isomaltulose
C01742
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4s)-3,4,5-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methoxy]oxane-3,4,5-triol
P1234
isomaltulose hydrate
SCHEMBL118910
(2r,3s,4s,5r,6s)-2-methylol-6-[[(2r,3s,4s)-3,4,5-trihydroxy-5-methylol-tetrahydrofuran-2-yl]methoxy]tetrahydropyran-3,4,5-triol
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4s)-5-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxolan-2-yl]methoxy]oxane-3,4,5-triol
J-006975
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(((2r,3s,4s)-3,4,5-trihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)methoxy)tetrahydro-2h-pyran-3,4,5-triol
Q27103048
STL565150
AKOS037623354
PD124262

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Both formulae were well accepted without differences in time of crying, flatulence, stool characteristics and the occurrence of adverse events."( Effects of a Follow-On Formula Containing Isomaltulose (Palatinose™) on Metabolic Response, Acceptance, Tolerance and Safety in Infants: A Randomized-Controlled Trial.
Demmelmair, H; Fleddermann, M; Holdt, L; Koletzko, B; Rauh-Pfeiffer, A; Teupser, D, 2016
)
0.43

Bioavailability

ExcerptReferenceRelevance
" We hypothesised that the reduced digestion and absorption rate of isomaltulose would result in lower glycaemic and insulinaemic responses when compared with the ingestion of sucrose, leading to greater postprandial fat oxidation rates."( Reduced glycaemic and insulinaemic responses following isomaltulose ingestion: implications for postprandial substrate use.
Blaak, EE; Brouns, F; Ijzerman, TH; van Can, JG; van Loon, LJ, 2009
)
0.35

Dosage Studied

ExcerptRelevanceReference
"Improved insulin sensitivity was significantly related to exercise dose in a graded dose-response relationship."( Exercise dose and insulin sensitivity: relevance for diabetes prevention.
Allison, KF; Amati, F; Dubé, JJ; Goodpaster, BH; Rousson, V, 2012
)
0.38
"This study identifies a graded dose-response relationship between exercise dose and improvements in insulin sensitivity."( Exercise dose and insulin sensitivity: relevance for diabetes prevention.
Allison, KF; Amati, F; Dubé, JJ; Goodpaster, BH; Rousson, V, 2012
)
0.38
" Three of these saccharides, having close and low-moderate degrees of hydrolysis by brush border enzymes, were also evaluated in vivo for their glycaemic effects by measuring plasma levels of glucose, insulin and glucagon-like peptide 1 (GLP-1) 0-180 min after administration of a single dosage after an overnight fast (i."( Brush border enzyme hydrolysis and glycaemic effects of isomaltulose compared to other saccharides in dogs.
Bosch, G; Corbee, RJ; de Jong, GAH; Mes, JJ; Neumer, F; Theis, S; van den Dool, RTM, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
sweetening agentSubstance that sweeten food, beverages, medications, etc.
animal metaboliteAny eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
glycosylfructose
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (187)

TimeframeStudies, This Drug (%)All Drugs %
pre-199031 (16.58)18.7374
1990's12 (6.42)18.2507
2000's47 (25.13)29.6817
2010's65 (34.76)24.3611
2020's32 (17.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials41 (21.35%)5.53%
Reviews11 (5.73%)6.00%
Case Studies1 (0.52%)4.05%
Observational0 (0.00%)0.25%
Other139 (72.40%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]