C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1N1C=CC2=C1N=C(F)N=C2N

InChIKey=DNJVIYGDUQKEIT-NBYAQTDISA-N

C12H15FN4O4

298.274

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 2-halopyrimidines Aminopyrimidines and derivatives Substituted pyrroles Aryl fluorides Imidolactams Tertiary alcohols Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Primary amines Organofluorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Aryl fluoride - Aryl halide - Monosaccharide - Pyrimidine - Substituted pyrrole - Imidolactam - Pyrrole - Tertiary alcohol - Heteroaromatic compound - Oxolane - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organofluoride - Organohalogen compound - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Amine - Primary amine - Alcohol - Organonitrogen compound - Organooxygen 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