C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1N1C=C(C(O)=O)C2=C1N=CN=C2N

InChIKey=KFTHWKFWOTUZDL-CZTVAOSCSA-N

C13H16N4O6

324.293

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrrolopyrimidine nucleosides and nucleotides

Not available

Not available

Pyrrolopyrimidine nucleosides and nucleotides

Glycosylamines Pyrrolo[2,3-d]pyrimidines Pyrrole carboxylic acids Aminopyrimidines and derivatives Substituted pyrroles Imidolactams Monosaccharides Vinylogous amides Tertiary alcohols Heteroaromatic compounds Oxolanes Secondary alcohols Amino acids Azacyclic compounds Oxacyclic compounds Carboxylic acids Primary amines Hydrocarbon derivatives Organic oxides Primary alcohols

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Pyrrole-3-carboxylic acid - Pyrrole-3-carboxylic acid or derivatives - Aminopyrimidine - Monosaccharide - Pyrimidine - Substituted pyrrole - Imidolactam - Oxolane - Heteroaromatic compound - Pyrrole - Tertiary alcohol - Vinylogous amide - Amino acid or derivatives - Secondary alcohol - Amino acid - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Carboxylic acid - Organonitrogen compound - Amine - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Alcohol - Primary alcohol - Primary amine - Hydrocarbon derivative - 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