Compound Identification
SMILES
NC1=NC2=C(N=CN2[C@@H]2C[C@@H](OS(N)(=O)=O)[C@@H](O)[C@H]2O)C(N)=N1
InChIKey
InChIKey=OKPSBDFQGCZICS-ZCBVHYEASA-N
Formula
C10H15N7O5S
Mass
345.33
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 Cyclitols and derivatives Organic sulfuric acids and derivatives Heteroaromatic compounds 1,2-diols Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Cyclitol or derivatives - Pyrimidine - Imidolactam - Cyclopentanol - Azole - Imidazole - Organic sulfuric acid or derivatives - Cyclic alcohol - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Azacycle - Organoheterocyclic compound - Primary amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Alcohol - Organooxygen compound - Organonitrogen 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