Page last updated: 2024-11-07

2,5-diketogluconic acid

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

Description

2,5-Diketogluconic acid (2,5-DKG) is a dicarboxylic acid derived from glucose. It is a potent chelator of metal ions, particularly iron, and has shown promise as a potential therapeutic agent for iron overload disorders. 2,5-DKG is synthesized through the oxidation of glucose using various enzymatic or chemical methods. Its ability to chelate iron has been investigated for its potential in treating iron overload conditions such as hemochromatosis and thalassemia. Additionally, 2,5-DKG exhibits antimicrobial activity against certain bacteria. Ongoing research focuses on exploring its potential applications in medicine, agriculture, and other fields.'

2,5-diketogluconic acid: RN given refers to (D-threo)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID102287
CHEBI ID18281
SCHEMBL ID379863
MeSH IDM0101693

Synonyms (18)

Synonym
2,5-dioxo-d-gluconic acid
CHEBI:18281
d-threo-hexo-2,5-diulosonic acid
2,5-didehydro-d-gluconic acid
2,5-diketo-d-gluconic acid
d-threo-2,5-hexodiulosonic acid
2595-33-7
C02780 ,
2,5-diketogluconic acid
hexo-2,5-diulosonic acid
(3s,4s)-3,4,6-trihydroxy-2,5-dioxohexanoic acid
einecs 219-992-3
RXMWXENJQAINCC-DMTCNVIQSA-N
SCHEMBL379863
LMFA01050471
DTXSID30936065
Q27102964
(3s,4s)-3,4,6-trihydroxy-2,5-dioxohexanoicacid
[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 (1)

ClassDescription
diketoaldonic acidDioxo carboxylic acids formally derived from aldoses by replacement of two secondary CHOH groups by carbonyl groups.
[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 (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (50.00)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)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: 12.23

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 Index12.23 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.18 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.23)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]