NC1=NC=NC2=C1C(=CN2C1OC(CO)C(O)C1O)C1=NCCCN1

InChIKey=MYVVSHFOJVHOSD-UHFFFAOYSA-N

C15H20N6O4

348.363

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 Aminopyrimidines and derivatives Substituted pyrroles Imidolactams Hydropyrimidines Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Carboxamidines Carboximidamides Hydrocarbon derivatives Organopnictogen compounds Primary alcohols Primary amines

Aromatic heteropolycyclic compounds

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Hydropyrimidine - 1,4,5,6-tetrahydropyrimidine - Monosaccharide - Pyrimidine - Substituted pyrrole - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Pyrrole - Secondary alcohol - Carboximidamide - Azacycle - Organoheterocyclic compound - Carboxylic acid amidine - Oxacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Amidine - Organic nitrogen compound - Amine - Organonitrogen compound - Alcohol - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Primary alcohol - Primary amine - 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