Compound Identification
SMILES
O[C@@H]1[C@@H](COC(C2=CC=CC=C2)C2=CC=CC=C2)O[C@H]([C@@H]1O)N1C=CC(=O)NC1=O
InChIKey
InChIKey=UFBUIPZDFBLBRU-XLBJILASSA-N
Formula
C22H22N2O6
Mass
410.426
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
Diphenylmethanes Glycosylamines Pentoses Benzylethers Pyrimidones Hydropyrimidines Vinylogous amides Heteroaromatic compounds Oxolanes Lactams 1,2-diols Secondary alcohols Ureas Azacyclic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Benzylether - Pyrimidone - Hydropyrimidine - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Pyrimidine - Vinylogous amide - Oxolane - Heteroaromatic compound - 1,2-diol - Lactam - Urea - Secondary alcohol - Dialkyl ether - Ether - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Alcohol - 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