Compound Identification
SMILES
NC1=NC(=S)C2=C(N1)N(C=N2)[C@@H]1O[C@@H](CO)[C@@H](O)[C@@H]1O
InChIKey
InChIKey=OTDJAMXESTUWLO-FULWYAMNSA-N
Formula
C10H13N5O4S
Mass
299.31
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 Purinethiones Pentoses Pyrimidinethiones Aminopyrimidines and derivatives Primary aromatic amines N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary alcohols Azacyclic compounds Oxacyclic compounds Organosulfur compounds Primary alcohols Hydrocarbon derivatives Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Purinethione - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidinethione - Primary aromatic amine - Monosaccharide - Pyrimidine - N-substituted imidazole - Imidazole - Oxolane - Azole - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Primary alcohol - 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