Compound Identification
SMILES
COCCOC1=NC2=C(NC(=O)N2C2CCCC2OCP(O)(O)=O)C(N)=N1
InChIKey
InChIKey=HQQGGBCJOVCIJF-UHFFFAOYSA-N
Formula
C14H22N5O7P
Mass
403.332
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
Purinones 6-aminopurines Aminopyrimidines and derivatives Alkyl aryl ethers N-substituted imidazoles Imidolactams Organic phosphonic acids Heteroaromatic compounds Ureas Dialkyl ethers Azacyclic compounds Primary amines Organophosphorus compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,2-substituted phosphonated cyclopentyl purine nucleoside - 6-aminopurine - Purinone - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - Imidolactam - Pyrimidine - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Organophosphonic acid - Organophosphonic acid derivative - Urea - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxide - Amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organophosphorus compound - Organooxygen compound - Organonitrogen 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