Compound Identification
SMILES
NC1=NC(=O)C2=C(N1)N(C1OC(CO)[C@@H](O)[C@H]1O)C(=O)N2CC(O)CSC1=CC=CC=C1
InChIKey
InChIKey=UQPZEGNDGUFSDM-OINXVUQXSA-N
Formula
C19H23N5O7S
Mass
465.48
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 Hypoxanthines Pentoses 6-oxopurines Thiophenol ethers Aminopyrimidines and derivatives Alkylarylthioethers Pyrimidones Benzene and substituted derivatives N-substituted imidazoles Oxolanes Heteroaromatic compounds Vinylogous amides Ureas Secondary alcohols 1,2-diols Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Primary alcohols Primary amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Purinone - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Pyrimidone - Alkylarylthioether - Benzenoid - Pyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - 1,2-diol - Thioether - Sulfenyl compound - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Alcohol - Primary alcohol - Organic nitrogen compound - Organosulfur compound - Organonitrogen compound - Organooxygen 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