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etheno-AMP

Known as: 3H-Imidazo(2,1-i)purine, 3-(5-O-phosphono-beta-D-ribofuranosyl)-, epsilon-AMP, etheno-adenosine monophosphate 
National Institutes of Health

Papers overview

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2011
2011
Exocyclic etheno-DNA adducts are formed by the reaction of lipid peroxidation products, such as 4-hydroxy-2-nonenal (HNE) with… 
2006
2006
Five major products (adducts A(1a), A(1b), A(2), A(3,) and B) from the reaction of guanosine (Guo) with 4-oxo-2(E)-nonenal (ONE… 
Highly Cited
2005
Highly Cited
2005
Analysis of the reaction between 4-hydroperoxy-2-nonenal (HPNE) and 2'-deoxyguanosine (dGuo) by liquid chromatography/mass… 
2005
2005
Reactive oxygen species convert the omega-6 polyunsaturated fatty acid arachidonic acid into 15-hydroperoxy-5,8,11,13-(Z,Z,ZE… 
Highly Cited
2004
Highly Cited
2004
Furan is an environmental chemical that induces liver toxicity and tumor formation in rodents, leading to its classification as a… 
Highly Cited
1999
Highly Cited
1999
Two major products (adducts A and B) from the reaction of 2-deoxyguanosine (dGuo) with 13-hydroperoxylinoleic acid were detected… 
Highly Cited
1998
Highly Cited
1998
In order to investigate specific DNA damage caused by nitric oxide (NO) induced lipid peroxidation, levels of promutagenic etheno…