CCNC(=O)C1=C(N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C2=C1C(NCC)=NC=N2)C1=CC=CC=C1

InChIKey=AUXWLQGNMSTWCT-JKWAKEATSA-N

C22H27N5O5

441.488

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrrolopyrimidine nucleosides and nucleotides

Not available

Not available

Pyrrolopyrimidine nucleosides and nucleotides

Glycosylamines Phenylpyrroles Pentoses Pyrrolo[2,3-d]pyrimidines Pyrimidinecarboxamides Pyrrole carboxamides Aminopyrimidines and derivatives Benzene and substituted derivatives Imidolactams Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Secondary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Amines Organic oxides

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - 2-phenylpyrrole - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrimidinecarboxamide - Pyrrolopyrimidine - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - Pyrimidine - Substituted pyrrole - Benzenoid - Imidolactam - Pyrrole - Heteroaromatic compound - Oxolane - Vinylogous amide - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Amine - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Primary alcohol - 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