Structure Information
Structure

Compound Identification

SMILES

NC1=C2N=CN([C@@H]3O[C@H](CSCCC(=O)C(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1

InChIKey

InChIKey=MXUWKYXWQUEGBX-QYVSTXNMSA-N

Formula

C14H17N5O6S

Mass

383.38

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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 - Imidazopyrimidine - Thia fatty acid - Hydroxy fatty acid - Fatty acyl - Imidolactam - Pyrimidine - N-substituted imidazole - Monosaccharide - Keto acid - Alpha-keto acid - Heteroaromatic compound - Tetrahydrofuran - 2-imidazoline - Azole - Alpha-hydroxy ketone - Amino acid - Secondary alcohol - Ketone - Amino acid or derivatives - Formamidine - Oxacycle - Azacycle - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Carboximidamide - Thioether - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Amidine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Alcohol - 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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