Compound Identification
SMILES
OC[C@H]1C[C@H](C=C1)N1C=NC2=C1N=C(NC1=C3C=C(F)C=CC3=NC1=O)N=C2NC1CC1
InChIKey
InChIKey=WFOCJQHTDPNHHP-RISCZKNCSA-N
Formula
C22H20FN7O2
Mass
433.447
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Cyclopentyl nucleosides
Intermediate Tree Nodes
1,3-substituted cyclopentyl nucleosides
Direct Parent
1,3-substituted cyclopentyl purine nucleosides
Alternative Parents
6-alkylaminopurines Alpha amino acids and derivatives Indoles and derivatives Aminopyrimidines and derivatives N-substituted imidazoles Aryl fluorides Imidolactams Benzenoids Heteroaromatic compounds N-acylimines Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Amines Organofluorides Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Alpha-amino acid or derivatives - Imidazopyrimidine - Indole or derivatives - Purine - Aminopyrimidine - Aryl fluoride - Aryl halide - Imidolactam - Benzenoid - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - N-acylimine - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Primary alcohol - Organohalogen compound - Organic oxygen compound - Organofluoride - Carbonyl group - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine 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 base.
External Descriptors
Not available