Structure Information
Structure

Compound Identification

SMILES

C[S+](CCC(N)C(O)=O)CC1OC(C(O)C1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=MEFKEPWMEQBLKI-UHFFFAOYSA-O

Formula

C15H23N6O5S

Mass

399.45

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