Compound Identification
SMILES
NC1=NC(=O)N(C=C1[Hg]Cl)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
InChIKey
InChIKey=DEBWUFGKLVMZFT-WFIJOQBCSA-M
Formula
C9H12ClHgN3O5
Mass
478.25
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 Pentoses Aminopyrimidines and derivatives Pyrimidones Hydropyrimidines Imidolactams Metal aryls Heteroaromatic compounds Oxolanes Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organic transition metal salts Organic oxides Primary alcohols Hydrocarbon derivatives Primary amines Organomercurial compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Metal aryl - Hydropyrimidine - Monosaccharide - Imidolactam - Pyrimidine - Heteroaromatic compound - Oxolane - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organic metal salt - Organic transition metal salt - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organometallic compound - Organomercurial-compound - Organic transition metal moeity - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Primary alcohol - Primary amine - 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