Structure Information
Structure

Compound Identification

SMILES

CCCOC(=O)[C@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N)NC(=O)COC

InChIKey

InChIKey=FRDUUZWLFIZOIU-NSDPQSHHSA-N

Formula

C20H30N6O7S

Mass

498.56

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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 - N-acyl-alpha amino acid or derivatives - Alpha-amino acid ester - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Fatty acid ester - Pyrimidine - Fatty acyl - Monosaccharide - N-substituted imidazole - Imidolactam - Azole - Oxolane - Imidazole - Heteroaromatic compound - Carboxylic acid ester - 1,2-diol - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkylthioether - Carboxylic acid derivative - Sulfenyl compound - Dialkyl ether - Ether - Thioether - Monocarboxylic acid or derivatives - Organic oxide - Carbonyl group - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organic oxygen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - 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

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