Page last updated: 2024-12-07

1,n(6)-ethenoadenine

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

Description

1,N(6)-ethenoadenine, also known as εA, is a **DNA adduct**, meaning it's a molecule that binds to DNA. This particular adduct is formed when **adenine**, one of the four DNA bases, reacts with **vinyl chloride**, a common industrial chemical.

Here's why it's important for research:

* **Cancer Research:** 1,N(6)-ethenoadenine is a **mutagenic** adduct, meaning it can cause changes in the DNA sequence. This can lead to the development of cancer. Research on εA helps us understand how vinyl chloride causes cancer and how to prevent or treat it.
* **Environmental Toxicology:** Vinyl chloride is a known environmental contaminant, and εA is a biomarker for exposure to this chemical. Studying this adduct helps us assess the risks of vinyl chloride exposure and develop strategies to minimize its harmful effects.
* **DNA Repair Mechanisms:** The presence of εA in DNA can trigger specific DNA repair pathways. Research on this adduct can help us understand how cells repair DNA damage and how to enhance these repair mechanisms to prevent disease.
* **Biomarker Development:** εA can be used as a biomarker to monitor exposure to vinyl chloride and assess the effectiveness of interventions aimed at reducing exposure.
* **Chemical Carcinogenesis:** εA serves as a model for studying how chemical carcinogens interact with DNA, leading to mutations and potentially cancer.

**In summary:** 1,N(6)-ethenoadenine is a crucial tool for research in cancer, environmental toxicology, DNA repair mechanisms, and biomarker development. Its presence in DNA highlights the dangers of vinyl chloride exposure and provides insights into the mechanisms of carcinogenesis.

1,N(6)-ethenoadenine: biologically active fluorescent derivatives of this cpd potentially valuable in studies concerning interactions between adenine cpds & various enzymes for which they serve as substrates or co-factors; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID104994
CHEBI ID29146
CHEBI ID42173
SCHEMBL ID4997669
SCHEMBL ID8127207
MeSH IDM0046231

Synonyms (28)

Synonym
BIDD:GT0038
ethenoadenine
1,n(6)-ethenoadenine
1h-imidazo[2,1-i]purine
13875-63-3
CHEBI:29146
3h-imidazo[2,1-i]purine
1,n6-ethenoadenine
CHEBI:42173
DB01952
1-n6-ethenoadenine
FT-0691075
1h-imidazo[2,1-f]purine
AKOS006273818
unii-sin7411hg7
sin7411hg7 ,
epsilona nucleobase
1h-imidazo(2,1-i)purine
SCHEMBL4997669
SCHEMBL8127207
DTXSID90160768
imidazo[2,1-i]purine
3h-imidazo[1,2-i]purine
Q27459874
.epsilon.-adenine
3h-imidazo(2,1-i)purine
1,n6-ethyleneadenine
PD060208
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
mutagenAn agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution.
[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
imidazo[2,1-i]purine
imidazo[2,1-i]purine
[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]

Pathways (5)

PathwayProteinsCompounds
DNA Repair25547
Base Excision Repair3523
Base-Excision Repair, AP Site Formation1716
Depurination107
Cleavage of the damaged purine47

Research

Studies (89)

TimeframeStudies, This Drug (%)All Drugs %
pre-199012 (13.48)18.7374
1990's30 (33.71)18.2507
2000's23 (25.84)29.6817
2010's21 (23.60)24.3611
2020's3 (3.37)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.22

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 Index10.22 (24.57)
Research Supply Index4.51 (2.92)
Research Growth Index4.73 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.22)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (1.12%)5.53%
Reviews6 (6.74%)6.00%
Case Studies1 (1.12%)4.05%
Observational1 (1.12%)0.25%
Other80 (89.89%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]