Compound Identification
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1C[C@H](COP(O)(=O)OC2=CC=CC=C2F)[C@H]1COP(O)(=O)OC1=CC=CC=C1F
InChIKey
InChIKey=XRAAXLLYLIDLOT-IIDMSEBBSA-N
Formula
C23H23F2N5O8P2
Mass
597.408
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 Fluorobenzenes Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Aryl fluorides Heteroaromatic compounds Azacyclic compounds Primary amines Organooxygen compounds Organofluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cyclobutyl purine nucleoside - Cyclobutyl nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Phenoxy compound - Aminopyrimidine - Fluorobenzene - Halobenzene - Monoalkyl phosphate - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Imidolactam - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organoheterocyclic compound - Organofluoride - Organic nitrogen compound - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Amine - Primary amine - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - 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