Compound Identification
SMILES
NC(=N)C1=CN([C@H]2O[C@@H](CO)[C@H](O)[C@@H]2O)C2=C1C(=O)N=CN2
InChIKey
InChIKey=CQVSGRBPWUXLOH-GVTXSBRZSA-N
Formula
C12H15N5O5
Mass
309.282
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 Pyrimidones Substituted pyrroles Oxolanes Heteroaromatic compounds Vinylogous amides 1,2-diols Secondary alcohols Oxacyclic compounds Carboximidamides Carboxamidines Azacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Pyrimidone - Monosaccharide - Pyrimidine - Substituted pyrrole - Oxolane - Heteroaromatic compound - Pyrrole - Vinylogous amide - Secondary alcohol - 1,2-diol - Azacycle - Amidine - Oxacycle - Carboximidamide - Organoheterocyclic compound - Carboxylic acid amidine - Alcohol - Organonitrogen compound - Organic oxide - Organic oxygen 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