Compound Identification
SMILES
C[C@]1(O[C@H](CO)C(O)[C@@H]1O)N1C=CC(N)=NC1=C
InChIKey
InChIKey=HJQMGZHGGAKUAR-GNTIEKQASA-N
Formula
C11H17N3O4
Mass
255.274
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
C-glycosyl compounds Pentoses Aminopyrimidines and derivatives Hydropyrimidines Imidolactams Oxolanes Ketene acetals Tertiary amines 1,2-diols Secondary alcohols Oxacyclic compounds Enamines Carboximidamides Carboxamidines Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Hydropyrimidine - 1,2-dihydropyrimidine - Imidolactam - Monosaccharide - Oxolane - 1,2-diol - Ketene acetal or derivatives - Tertiary amine - Secondary alcohol - Amidine - Carboxylic acid amidine - Enamine - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Amine - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aliphatic 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