Structure Information
Structure

Compound Identification

SMILES

N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1NC=NC2=O)C(O)=O

InChIKey

InChIKey=VNPWVMVYUSNFAW-WFMPWKQPSA-N

Formula

C14H19N5O6S

Mass

385.4

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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 - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Hypoxanthine - Purine - Imidazopyrimidine - Pyrimidone - Thia fatty acid - Hydroxy fatty acid - Pyrimidine - N-substituted imidazole - Monosaccharide - Fatty acyl - Heteroaromatic compound - Imidazole - Azole - Tetrahydrofuran - Vinylogous amide - Secondary alcohol - Amino acid or derivatives - Amino acid - 1,2-diol - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Dialkylthioether - Sulfenyl compound - Thioether - Monocarboxylic acid or derivatives - Organic oxide - Organopnictogen compound - Alcohol - Organic oxygen compound - Carbonyl group - Amine - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Organic nitrogen compound - 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

CHEBI:17010 : homocysteines

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