Compound Identification
SMILES
NC1=NC(=O)N(C=C1F)[C@H]1O[C@@H](CO)C=C1.CC1=CN([C@@H]2O[C@](CO)(C=C2)C#C)C(=O)NC1=O
InChIKey
InChIKey=DNTIJIWLVMXYLF-MHRKJDEOSA-N
Formula
C21H22FN5O7
Mass
475.433
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Nucleoside and nucleotide analogues
Alternative Parents
Aminopyrimidines and derivatives Pyrimidones Halopyrimidines Ynones Aryl fluorides Hydropyrimidines Imidolactams Vinylogous amides Dihydrofurans Heteroaromatic compounds Ureas Lactams Oxacyclic compounds Azacyclic compounds Acetylides Organofluorides Hydrocarbon derivatives Organopnictogen compounds Primary alcohols Primary amines Organic oxides
Molecular Framework
Not available
Substituents
Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Pyrimidine - Ynone - Imidolactam - Vinylogous amide - Heteroaromatic compound - Dihydrofuran - Urea - Lactam - Organoheterocyclic compound - Acetylide - Oxacycle - Azacycle - Amine - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Primary alcohol - Organic nitrogen compound - Organic oxygen compound - Primary amine - Organopnictogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.
External Descriptors
Not available