Compound Identification
SMILES
NC1=NC(=NC2=C1N=CN2C1OC(COS(N)(=O)=O)C(O)C1O)C#C
InChIKey
InChIKey=LRSLPIPDJFGDOM-UHFFFAOYSA-N
Formula
C12H14N6O6S
Mass
370.34
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Purine nucleosides
Alternative Parents
Glycosylamines Pentoses 6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Organic sulfuric acids and derivatives Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Acetylides Azacyclic compounds Organopnictogen compounds Primary amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Monosaccharide - Imidolactam - Pyrimidine - N-substituted imidazole - Imidazole - Tetrahydrofuran - Organic sulfuric acid or derivatives - Heteroaromatic compound - Azole - 1,2-diol - Secondary alcohol - Acetylide - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Amine - Primary amine - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available