Compound Identification
SMILES
CC(C)OP(=O)(CO[C@@H]1CCC[C@H]1N1C=NC2=C1N=CN=C2N)OC(C)C
InChIKey
InChIKey=WADKQMXGGNADCH-ZIAGYGMSSA-N
Formula
C17H28N5O4P
Mass
397.416
Taxonomic Classification
Taxonomy Tree
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Phosphonated cyclopentyl nucleosides
Intermediate Tree Nodes
1,2-substituted phosphonated cyclopentyl nucleosides
Direct Parent
1,2-substituted phosphonated cyclopentyl purine nucleosides
Alternative Parents
6-aminopurines Dialkyl alkylphosphonates Aminopyrimidines and derivatives Phosphonic acid esters N-substituted imidazoles Imidolactams Heteroaromatic compounds Azacyclic compounds Primary amines Organophosphorus compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,2-substituted phosphonated cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl alkylphosphonate - Phosphonic acid diester - N-substituted imidazole - Imidolactam - Pyrimidine - Phosphonic acid ester - Azole - Imidazole - Heteroaromatic compound - Organophosphonic acid derivative - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Primary amine - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organophosphorus compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1,2-substituted phosphonated cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 2-position with either a purine base.
External Descriptors
Not available