Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(SC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)C=C1

InChIKey

InChIKey=YPBFMIZDPCDUOG-LSCFUAHRSA-N

Formula

C17H19N5O4S

Mass

389.43

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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 - Imidazopyrimidine - Purine - Anisole - Phenoxy compound - Aryl thioether - Phenol ether - Thiophenol ether - Methoxybenzene - Aminopyrimidine - Alkylarylthioether - Alkyl aryl ether - Benzenoid - Imidolactam - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Oxolane - Heteroaromatic compound - Imidazole - Azole - Secondary alcohol - 1,2-diol - Thioether - Sulfenyl compound - Azacycle - Organoheterocyclic compound - Oxacycle - Ether - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Organic oxygen compound - Amine - Primary amine - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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

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