Compound Identification
SMILES
CCOP(=O)(COC1CC(CC1O)N1C=C(C)C(O)=NC1=O)OCC
InChIKey
InChIKey=CEEVPDLZRBSVGO-UHFFFAOYSA-N
Formula
C15H25N2O7P
Mass
376.346
Taxonomic Classification
Taxonomy Tree
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Phosphonated cyclopentyl nucleosides
Intermediate Tree Nodes
1,3-substituted phosphonated cyclopentyl nucleosides
Direct Parent
1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides
Alternative Parents
Cyclopentyl nucleosides Pyrimidones Hydroxypyrimidines Dialkyl alkylphosphonates Phosphonic acid esters Hydropyrimidines Cyclopentanols Heteroaromatic compounds Cyclic alcohols and derivatives Azacyclic compounds Organopnictogen compounds Organophosphorus compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
1,3-substituted phosphonated cyclopentyl pyrimidine nucleoside - Cyclopentyl nucleoside - Dialkyl alkylphosphonate - Hydroxypyrimidine - Phosphonic acid diester - Pyrimidone - Cyclopentanol - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Cyclic alcohol - Organophosphonic acid derivative - Heteroaromatic compound - Secondary alcohol - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 1,3-substituted phosphonated cyclopentyl pyrimidine 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 3-position with either a pyrimidine base.
External Descriptors
Not available