Page last updated: 2024-12-05

glycinaldehyde

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

Description

Glycinaldehyde is a sugar-derived aldehyde, a reactive species of particular interest in biological chemistry. It has been proposed to play a role in various biological processes, including glycosylation, protein modification, and antioxidant defense. Glycinaldehyde can be formed through the degradation of carbohydrates, particularly fructose, and is known to react with DNA, forming adducts that can damage genetic material. Its formation has also been linked to oxidative stress, a factor in aging and certain diseases. The study of glycinaldehyde focuses on understanding its reactivity, its role in biological systems, and its potential impact on health. Research includes investigating its mechanisms of formation, its interaction with biomolecules, and its potential therapeutic applications. '

glycinaldehyde: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID13002
CHEBI ID82332
MeSH IDM0051324

Synonyms (45)

Synonym
glycidaldehyde [un2622] [flammable liquid]
5-17-09-00006 (beilstein handbook reference)
unii-kys59r58sk
kys59r58sk ,
oxirane-2-carbaldehyde
2,3-epoxypropionaldehyde
epihydrinaldehyde
propionaldehyde,3-epoxy-
glycidaldehyde
nsc-521506
oxiranecarboxaldehyde
nsc521506
2,3-epoxy-1-propanal
765-34-4
2,3-epoxypropanal
wln: t3otj bvh
glycidal
epihydrine aldehyde
ai3-26165
rcra waste no. u126
oxirane-carboxaldehyde
einecs 212-143-8
rcra waste number u126
un2622
glycinaldehyde
ccris 319
nsc 521506
epoxypropanal
formyloxiran
brn 0103970
propionaldehyde, 2,3-epoxy-
glycidylaldehyde
hsdb 5100
AKOS006278467
2-oxiranecarboxaldehyde
C19246
glycidaldehyde [iarc]
glycinaldehyde [hsdb]
formyloxirane
CHEBI:82332
DTXSID9020665
epihydrinaldehyd
glycialdehyde
Q2307855
EN300-103531
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
epoxideAny cyclic ether in which the oxygen atom forms part of a 3-membered ring.
[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 (21)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (47.62)18.7374
1990's4 (19.05)18.2507
2000's6 (28.57)29.6817
2010's1 (4.76)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.07

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.07 (24.57)
Research Supply Index3.18 (2.92)
Research Growth Index4.25 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.07)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (4.55%)5.53%
Reviews1 (4.55%)6.00%
Case Studies1 (4.55%)4.05%
Observational0 (0.00%)0.25%
Other19 (86.36%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]