C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1N1C=C(Cl)C2=C1NC(N)=NC2=O

InChIKey=FIUAEQMATQPHRT-GSWPYSDESA-N

C12H15ClN4O5

330.73

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrrolopyrimidine nucleosides and nucleotides

Not available

Not available

Pyrrolopyrimidine nucleosides and nucleotides

Glycosylamines Pyrrolo[2,3-d]pyrimidines Aminopyrimidines and derivatives Pyrimidones Substituted pyrroles Aryl chlorides Monosaccharides Vinylogous halides Vinylogous amides Tertiary alcohols Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Organochlorides Hydrocarbon derivatives Primary alcohols Primary amines Organic oxides

Aromatic heteropolycyclic compounds

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