Page last updated: 2024-11-11

fructosyl-lysine

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

Description

fructosyllysine : A glyco-amino acid consisting of a D-fructosyl residue attached to the epsilon-amino group of L-lysine. [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 CID9839580
CHEBI ID24109
SCHEMBL ID1115953
MeSH IDM0103108

Synonyms (24)

Synonym
fructosyl-lysine
epsilon-fructoselysine
epsilon-fructosyl-l-lysine
n(6)-(1-deoxy-d-fructos-1-yl)-l-lysine
1-{[(5s)-5-amino-5-carboxypentyl]amino}-1-deoxy-d-fructose
fructose lysine
21291-40-7
CHEBI:24109
fructosyllysine
unii-f2rds6j0y0
l-lysine, n6-(1-deoxy-d-fructos-1-yl)-
f2rds6j0y0 ,
SCHEMBL1115953
1-deoxy-1-(.epsilon.-n-l-lysino)-d-fructose
.epsilon.-n-deoxyfructosyllysine
n.epsilon.-(1-deoxy-d-fructos-1-yl)-l-lysine
.epsilon.-fructoselysine
Q25101009
HY-129380
(2s)-2-amino-6-[[(3s,4r,5r)-3,4,5,6-tetrahydroxy-2-oxohexyl]amino]hexanoic acid
CS-0105134
n6-((3s,4r,5r)-3,4,5,6-tetrahydroxy-2-oxohexyl)-l-lysine
DTXSID301045836
AKOS040741768

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
"Determination of the consequences of a high level of lactuloselysine in milk on the bioavailability of skim milk nutrients and the kinetics of their appearance in the portal blood and of their urinary and faecal excretions and extrapolation to lower heat treatments and to man, using the pig model."( Nutritional and metabolic consequences of the early Maillard reaction of heat treated milk in the pig. Significance for man.
Calmes, R; Finot, PA; RĂ©rat, A; Vaissade, P, 2002
)
0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
[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 (2)

ClassDescription
fructosamine
glyco-amino acid
[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 (94)

TimeframeStudies, This Drug (%)All Drugs %
pre-19909 (9.57)18.7374
1990's23 (24.47)18.2507
2000's37 (39.36)29.6817
2010's20 (21.28)24.3611
2020's5 (5.32)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 19.50

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index19.50 (24.57)
Research Supply Index4.61 (2.92)
Research Growth Index4.81 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (19.50)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (3.13%)5.53%
Reviews2 (2.08%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other91 (94.79%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]