Compound Identification
SMILES
OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=C(OC2=CC=CC=C2)C(=O)NC1=O
InChIKey
InChIKey=JIDPXILNKWTMNY-MNXVOIDGSA-N
Formula
C15H16N2O7
Mass
336.3
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
Diarylethers Glycosylamines Pentoses Phenol ethers Phenoxy compounds Pyrimidones Hydropyrimidines Tetrahydrofurans Heteroaromatic compounds Vinylogous amides Secondary alcohols Lactams Ureas Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Diaryl ether - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Phenoxy compound - Phenol ether - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Benzenoid - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Lactam - Urea - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - 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