N\C(=N\O)C1=CN([C@H]2O[C@@H](CO)[C@H](O)[C@H]2O)C2=C1C(NO)=NC=N2

InChIKey=VDRNYDUPTSTUEE-NBFDCZBZSA-N

C12H16N6O6

340.296

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrrolopyrimidine nucleosides and nucleotides

Not available

Not available

Pyrrolopyrimidine nucleosides and nucleotides

Glycosylamines Pentoses Pyrrolo[2,3-d]pyrimidines Arylhydroxamates Substituted pyrroles Pyrimidines and pyrimidine derivatives Imidolactams Amidoximes Heteroaromatic compounds Oxolanes Secondary alcohols Azacyclic compounds N-organohydroxylamines Oxacyclic compounds Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Arylhydroxamate - Monosaccharide - Pyrimidine - Imidolactam - Substituted pyrrole - Amidoxime - Heteroaromatic compound - Oxolane - Pyrrole - Secondary alcohol - Amidine - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Primary alcohol - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as pyrrolopyrimidine nucleosides and nucleotides. These are nucleoside derivatives containing a ribose derivative which is n-glycosylated to a pyrrolopyrimidine. Also called deazapurine nucleosides, they are analogs of purine nucleosides with the N atom of the purine being replaced by a C atom at position 7.

Not available