Title : Modeling the conformational preference of the carbon-bonded covalent adduct formed upon exposure of 2'-deoxyguanosine to ochratoxin A.

Pub. Date : 2013 May 20

PMID : 23560542






1 Functional Relationships(s)
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1 A focus was placed on the influence of the C8-modification of 2"-deoxyguanosine (dG) on the preferred relative arrangement of the nucleobase and the C8-substituent and, more importantly, the anti/syn conformational preference with respect to the glycosidic bond. Deoxyguanosine synemin Homo sapiens