Compound Identification
SMILES
NC1=NC(=O)C2=C(N1)N(C=C2CCC1=CC=CC=C1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
InChIKey
InChIKey=VPZJSJUJYPNPOO-SCFUHWHPSA-N
Formula
C19H24N4O11P2
Mass
546.366
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
Pentose phosphates Glycosylamines Monosaccharide phosphates Organic pyrophosphates Pyrrolo[2,3-d]pyrimidines Aminopyrimidines and derivatives Monoalkyl phosphates Pyrimidones Substituted pyrroles Benzene and substituted derivatives Heteroaromatic compounds Vinylogous amides Oxolanes Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Monocyclic benzene moiety - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Benzenoid - Substituted pyrrole - Alkyl phosphate - Oxolane - Pyrrole - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Organic oxide - Alcohol - Hydrocarbon derivative - Primary amine - Amine - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen 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