Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(NC(CSC[C@H]3OC([C@H](O)[C@@H]3O)N3C=NC4=C3N=CN=C4N)=C2)N1

InChIKey

InChIKey=SQLQZCWJQHPUAV-ITAOHXQZSA-N

Formula

C17H19N9O4S

Mass

445.46

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

5'-deoxy-5'-thionucleosides

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxy-5'-thionucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxy-5'-thionucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Imidazopyrimidine - Purine - Pyrrolopyrimidine - Aminopyrimidine - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Substituted pyrrole - Imidolactam - Vinylogous amide - Pyrrole - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Dialkylthioether - Azacycle - Sulfenyl compound - Oxacycle - Thioether - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Amine - Organosulfur compound - Primary amine - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxy-5'-thionucleosides. These are 5'-deoxyribonucleosides in which the ribose is thio-substituted at the 5'position by a S-alkyl group.

External Descriptors

Not available

Previous Back Next