Compound Identification
SMILES
OCC1CC(C(O)C1O)N1C=NC2=C1N=CN=C2Cl
InChIKey
InChIKey=GGJDZOWNXFYEEV-UHFFFAOYSA-N
Formula
C11H13ClN4O3
Mass
284.7
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
Purines and purine derivatives Halopyrimidines N-substituted imidazoles Cyclopentanols Aryl chlorides Heteroaromatic compounds Cyclic alcohols and derivatives Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-substituted cyclopentyl purine nucleoside - Purine - Imidazopyrimidine - Halopyrimidine - Pyrimidine - N-substituted imidazole - Cyclopentanol - Aryl halide - Aryl chloride - Heteroaromatic compound - Imidazole - Cyclic alcohol - Azole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Alcohol - 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