Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2C1CC(CO)C1COP(O)(=O)OC1=CC=C(Cl)C=C1
InChIKey
InChIKey=OWGJUDRWGPTXMB-UHFFFAOYSA-N
Formula
C17H19ClN5O5P
Mass
439.79
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Nucleoside and nucleotide analogues
- Subclass Cyclobutyl nucleosides
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Cyclobutyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclobutyl nucleosides
Alternative Parents
6-aminopurines Phenoxy compounds Monoalkyl phosphates Chlorobenzenes Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary amines Primary alcohols Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cyclobutyl purine nucleoside - Cyclobutyl nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Phenoxy compound - Aminopyrimidine - Chlorobenzene - Halobenzene - Monoalkyl phosphate - Benzenoid - Alkyl phosphate - Pyrimidine - Imidolactam - Aryl chloride - Phosphoric acid ester - Aryl halide - Monocyclic benzene moiety - Organic phosphoric acid derivative - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organohalogen compound - Amine - Alcohol - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Organic oxide - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as cyclobutyl nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3- position with either a purine or pyrimidine base.
External Descriptors
Not available