Compound Identification
SMILES
CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCNC(=O)C(F)(F)F)C(=O)N=C1
InChIKey
InChIKey=YGIWQTHVVVHAOK-GWOFURMSSA-N
Formula
C14H18F3N3O6
Mass
381.308
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Pyrimidine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrimidine nucleosides
Alternative Parents
Glycosylamines Pyrimidones Hydropyrimidines Monosaccharides Heteroaromatic compounds Oxolanes Secondary alcohols Secondary carboxylic acid amides Dialkyl ethers Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Organofluorides Organic oxides Primary alcohols Hydrocarbon derivatives Alkyl fluorides Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Heteroaromatic compound - Oxolane - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Alcohol - Organofluoride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Primary alcohol - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available