Compound Identification
SMILES
OCC1(CO)CC2C=CC1C2N1C=NC2=C1N=CN=C2Cl
InChIKey
InChIKey=JTFQNWOUDPMEGD-UHFFFAOYSA-N
Formula
C14H15ClN4O2
Mass
306.75
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 Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-substituted cyclopentyl purine nucleoside - Imidazopyrimidine - Purine - Halopyrimidine - Pyrimidine - Aryl chloride - Aryl halide - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organic nitrogen compound - Organonitrogen compound - Alcohol - Organooxygen compound - Primary alcohol - Organic oxygen compound - 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