Compound Identification
SMILES
NCC1=CN(C2OC(CO)C(O)C2O)C2=C1C(N)=NC=N2
InChIKey
InChIKey=AFMKIRMZLLCSAV-UHFFFAOYSA-N
Formula
C12H17N5O4
Mass
295.299
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 Aminopyrimidines and derivatives Aralkylamines Substituted pyrroles Imidolactams Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols Monoalkylamines Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Aralkylamine - Imidolactam - Substituted pyrrole - Pyrimidine - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - Pyrrole - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Amine - Primary alcohol - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - 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