CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC2=C1N=C(N)N=C2Cl

InChIKey=RAKFNXONRBHUQJ-KCGFPETGSA-N

C12H15ClN4O4

314.73

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 Halopyrimidines Substituted pyrroles Aryl chlorides Monosaccharides Heteroaromatic compounds Oxolanes Secondary alcohols Azacyclic compounds Dialkyl ethers Oxacyclic compounds Organochlorides Hydrocarbon derivatives Primary amines Primary alcohols

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Substituted pyrrole - Pyrimidine - Monosaccharide - Heteroaromatic compound - Pyrrole - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Primary amine - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - 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