Compound Identification
SMILES
CCOP(=O)(COC1CC(C=C1)N1C=CC(N=CN(C)C)=NC1=O)OCC
InChIKey
InChIKey=IMSUGPHBXNDJFS-UHFFFAOYSA-N
Formula
C17H27N4O5P
Mass
398.4
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
Pyrimidones Dialkyl alkylphosphonates Phosphonic acid esters Hydropyrimidines Heteroaromatic compounds Tertiary amines Propargyl-type 1,3-dipolar organic compounds Formamidines Carboxamidines Azacyclic compounds Organophosphorus compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
1,3-substituted phosphonated cyclopentyl pyrimidine nucleoside - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Organophosphonic acid derivative - Heteroaromatic compound - Tertiary amine - Amidine - Carboxylic acid amidine - Formamidine - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organophosphorus compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organonitrogen 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