Compound Identification
SMILES
CSC1=NC(N)=NC2=C1N=CN2C1CC(CO)C=C1
InChIKey
InChIKey=PQNJVTOQOVXZMZ-UHFFFAOYSA-N
Formula
C12H15N5OS
Mass
277.35
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Cyclopentyl nucleosides
Intermediate Tree Nodes
1,3-substituted cyclopentyl nucleosides
Direct Parent
1,3-substituted cyclopentyl purine nucleosides
Alternative Parents
6-thiopurines Aminopyrimidines and derivatives Alkylarylthioethers N-substituted imidazoles Heteroaromatic compounds Sulfenyl compounds Azacyclic compounds Primary amines Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-substituted cyclopentyl purine nucleoside - 6-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Aminopyrimidine - Alkylarylthioether - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Primary amine - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine base.
External Descriptors
Not available