Compound Identification
SMILES
NCCCNC(=O)C1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C2=C1C(=O)N=C(N)N2
InChIKey
InChIKey=QZPUBMFQBWPQJT-AKAIJSEGSA-N
Formula
C15H22N6O6
Mass
382.377
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 Pyrimidinecarboxamides Pyrrolo[2,3-d]pyrimidines Pyrrole carboxamides Aminopyrimidines and derivatives Pyrimidones Substituted pyrroles Oxolanes Heteroaromatic compounds Vinylogous amides Amino acids and derivatives Secondary alcohols Secondary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Primary alcohols Organic oxides Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrimidinecarboxamide - Pyrrolopyrimidine - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Aminopyrimidine - Pyrimidone - Monosaccharide - Pyrimidine - Substituted pyrrole - Oxolane - Heteroaromatic compound - Vinylogous amide - Pyrrole - Secondary alcohol - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Primary amine - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Organic oxygen compound - Organooxygen compound - Alcohol - Amine - Primary alcohol - Organic nitrogen compound - 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