Structure Information
Structure

Compound Identification

SMILES

COC1=CC2=C(SC(SC[C@H]3OC([C@H](O)[C@@H]3O)N3C=NC4=C3N=CN=C4NC3CCCC3)=N2)C=C1

InChIKey

InChIKey=UOFDOFHVLICLSM-CRWZYULMSA-N

Formula

C23H26N6O4S2

Mass

514.62

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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-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - 1,3-benzothiazole - Imidazopyrimidine - Purine - Anisole - Aryl thioether - Phenol ether - Alkylarylthioether - Alkyl aryl ether - Aminopyrimidine - Secondary aliphatic/aromatic amine - Imidolactam - Benzenoid - Monosaccharide - N-substituted imidazole - Pyrimidine - Thiazole - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Secondary amine - Oxacycle - Azacycle - Thioether - Ether - Sulfenyl compound - Organoheterocyclic compound - Organooxygen compound - Organic nitrogen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - 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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