Compound Identification
SMILES
CCNC1=NC=NC2=C1C(=CN2C1OC(CO)C(O)C1O)C(N)=S
InChIKey
InChIKey=PAWWDDISIGPSJH-UHFFFAOYSA-N
Formula
C14H19N5O4S
Mass
353.4
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 Imidolactams Substituted pyrroles Heteroaromatic compounds Thioamides Oxolanes Secondary alcohols Oxacyclic compounds Thiocarboxylic acid amides Azacyclic compounds Hydrocarbon derivatives Amines Thiocarbonyl compounds Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Monosaccharide - Pyrimidine - Substituted pyrrole - Imidolactam - Oxolane - Thioamide - Heteroaromatic compound - Pyrrole - Secondary alcohol - Organoheterocyclic compound - Azacycle - Thiocarboxylic acid amide - Oxacycle - Thiocarbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Amine - 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