Structure Information
Structure

Compound Identification

SMILES

CC#CC[S+](CC[C@H](N)C(O)=O)C[C@H]1O[C@H](C(O)[C@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=FYSSPXIGESSXOC-WHZVBYNISA-O

Formula

C18H25N6O5S

Mass

437.49

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