Compound Identification
SMILES
NC1=NC(=O)C2=C(N1)N([C@H]1C[C@H](O)[C@@H](CO)O1)C(NC1=CC3=C(C=C1)C1=C(C3)C=C(F)C=C1)=N2
InChIKey
InChIKey=YJIAIUPBEIZQNN-RCCFBDPRSA-N
Formula
C23H21FN6O4
Mass
464.457
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
-
Class
Purine nucleosides
- Subclass Purine 2'-deoxyribonucleosides
-
Class
Purine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Purine 2'-deoxyribonucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Purine 2'-deoxyribonucleosides
Alternative Parents
Fluorenes 6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives Aminoimidazoles Aryl fluorides N-substituted imidazoles Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Secondary amines Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organofluorides Organopnictogen compounds Primary alcohols Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine 2'-deoxyribonucleoside - Fluorene - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Aminoimidazole - Aryl fluoride - Aryl halide - N-substituted imidazole - Pyrimidine - Benzenoid - Vinylogous amide - Heteroaromatic compound - Tetrahydrofuran - Azole - Imidazole - Secondary alcohol - Azacycle - Oxacycle - Secondary amine - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organic oxide - Organopnictogen compound - Organofluoride - Amine - Alcohol - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.
External Descriptors
Not available