Structure Information
Structure

Compound Identification

SMILES

NC(CCSCC1OC(C(O)C1O)N1C=NC2=C1N=CN=C2NCC1=CC=CC=C1)C(O)=O

InChIKey

InChIKey=LCMRXADLVDEDPG-UHFFFAOYSA-N

Formula

C21H26N6O5S

Mass

474.54

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