Compound Identification
SMILES
CCC(C)OP(O)(=O)COC1CCCC1N1C=NC2=C1N=C(OCCOC)N=C2N
InChIKey
InChIKey=KIOLNCSRYFCXMK-UHFFFAOYSA-N
Formula
C18H30N5O6P
Mass
443.441
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 Aminopyrimidines and derivatives Alkyl aryl ethers Phosphonic acid esters N-substituted imidazoles Imidolactams Organic phosphonic acids Heteroaromatic compounds 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 - Imidazopyrimidine - Purine - Alkyl aryl ether - Aminopyrimidine - Imidolactam - Pyrimidine - N-substituted imidazole - Phosphonic acid ester - Azole - Heteroaromatic compound - Imidazole - Organophosphonic acid - Organophosphonic acid derivative - 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