Compound Identification
SMILES
COC1=NC=NC2=C1C(I)=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
InChIKey
InChIKey=HPLISFULQJAEBT-WOUKDFQISA-N
Formula
C12H14IN3O5
Mass
407.164
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 Alkyl aryl ethers Substituted pyrroles Aryl iodides Pyrimidines and pyrimidine derivatives Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Azacyclic compounds Oxacyclic compounds Organonitrogen compounds Organoiodides Hydrocarbon derivatives Primary alcohols Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Alkyl aryl ether - Aryl halide - Aryl iodide - Monosaccharide - Pyrimidine - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Tetrahydrofuran - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Ether - Alcohol - Organoiodide - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Hydrocarbon derivative - Primary alcohol - 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