NC1=NC(=O)C2=C(N1)N(C1O[C@H](CO)[C@@H](O)[C@H]1O)C(Cl)=C2

InChIKey=FTECXQMVWOMEJW-VTHZCTBJSA-N

C11H13ClN4O5

316.7

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 Pyrimidones Aminopyrimidines and derivatives Substituted pyrroles Aryl chlorides Vinylogous amides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organochlorides Primary alcohols Primary amines Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Pyrimidone - Aryl chloride - Aryl halide - Monosaccharide - Pyrimidine - Substituted pyrrole - Heteroaromatic compound - Oxolane - Vinylogous amide - Pyrrole - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Amine - Organic nitrogen 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