Compound Identification
SMILES
CN(C)C1=NC=NC2=C1C=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@@]1(C)O
InChIKey
InChIKey=BNSCOVDUHDURAI-DMTCVQMQSA-N
Formula
C14H20N4O4
Mass
308.338
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrrolopyrimidine nucleosides and nucleotides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrrolopyrimidine nucleosides and nucleotides
Alternative Parents
Glycosylamines Pentoses Pyrrolo[2,3-d]pyrimidines Dialkylarylamines Aminopyrimidines and derivatives Substituted pyrroles Imidolactams Tertiary alcohols Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Dialkylarylamine - Aminopyrimidine - Imidolactam - Substituted pyrrole - Pyrimidine - Monosaccharide - Tertiary alcohol - Heteroaromatic compound - Pyrrole - Oxolane - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Amine - Aromatic heteropolycyclic compound
Description
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.
External Descriptors
Not available