Structure Information
Structure

Compound Identification

SMILES

NS(=O)(=O)C1=CC=C(C=C1)S(=O)(=O)NC1=CC=CC2=C1NC=C2Cl.CCCCCOC(=O)NC1=NC(=O)N(C=C1F)[C@@H]1O[C@H](C)[C@@H](O)[C@H]1O

InChIKey

InChIKey=MOQLDJXGSYSWAU-HZKBADDRSA-N

Formula

C29H34ClFN6O10S2

Mass

745.19

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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

Not available

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Indole - Indole or derivatives - Halopyrimidine - Pyrimidone - Hydropyrimidine - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Aryl chloride - Pyrimidine - Substituted pyrrole - Organosulfonic acid amide - Benzenoid - Pyrrole - Heteroaromatic compound - Oxolane - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Secondary alcohol - 1,2-diol - Carboximidic acid derivative - Azacycle - Oxacycle - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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

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