Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)C[C@H]1OC([C@@H](O)[C@H]1O)N1C=NC2=C1N=CN=C2NNC1=CC=C(C=C1)S(N)(=O)=O

InChIKey

InChIKey=FJFFAMCWDIHKBJ-HWQOSGRBSA-N

Formula

C19H24N8O6S

Mass

492.51

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Benzenesulfonamide - Imidazopyrimidine - Purine - Benzenesulfonyl group - Phenylhydrazine - N-substituted imidazole - Monosaccharide - Pyrimidine - Organosulfonic acid amide - Benzenoid - Imidolactam - Monocyclic benzene moiety - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Imidazole - Sulfonyl - Aminosulfonyl compound - Oxolane - Heteroaromatic compound - Azole - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic nitrogen compound - Hydrazine derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

Previous Back Next