Compound Identification
SMILES
NC1C(CO)CC(C1O)N1C=NC2=C1N=CN=C2N
InChIKey
InChIKey=WYMIIYMQKKFLES-UHFFFAOYSA-N
Formula
C11H16N6O2
Mass
264.289
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-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Cyclopentanols Heteroaromatic compounds 1,3-aminoalcohols Cyclic alcohols and derivatives 1,2-aminoalcohols Azacyclic compounds Primary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Cyclopentanol - N-substituted imidazole - Pyrimidine - Imidolactam - 1,3-aminoalcohol - Azole - Cyclic alcohol - Imidazole - Heteroaromatic compound - 1,2-aminoalcohol - Secondary alcohol - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Hydrocarbon derivative - Alcohol - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Primary 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