Compound Identification
SMILES
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(NCCC2C=NC3=CC=CC=C23)=NC1=O
InChIKey
InChIKey=YVUOXQGMLOFTGA-BQWVQBOQSA-N
Formula
C20H24N4O5
Mass
400.435
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Pyrimidine nucleosides
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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 3-alkylindoles Pyrimidones Aminopyrimidines and derivatives Monosaccharides Imidolactams Hydropyrimidines Benzenoids Tertiary alcohols Oxolanes Heteroaromatic compounds Secondary alcohols Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Imines Organic oxides Amines Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - 3-alkylindole - Indole - Indole or derivatives - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Benzenoid - Imidolactam - Tertiary alcohol - Oxolane - Heteroaromatic compound - Secondary alcohol - Azacycle - Organic 1,3-dipolar compound - Oxacycle - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic oxygen compound - Amine - Organonitrogen compound - Hydrocarbon derivative - Imine - Alcohol - Organic oxide - Organooxygen compound - Primary alcohol - Organic nitrogen compound - Aromatic heteropolycyclic 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