Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=ZJUKTBDSGOFHSH-UVKVXARGSA-N

Formula

C14H20N6O5S

Mass

384.41

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