Structure Information
Structure

Compound Identification

SMILES

O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CNS(=O)(=O)C1=CC=C(C=C1)C(=O)N\N=C\C1=C(C=CC=C1Cl)[N+]([O-])=O)N1C=CC(=O)NC1=O

InChIKey

InChIKey=DWQMBDIHHFTSIW-GIHQUTIZSA-N

Formula

C23H21ClN6O10S

Mass

608.96

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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

Aromatic heteromonocyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Benzenesulfonamide - Pentose monosaccharide - Benzoic acid or derivatives - Benzenesulfonyl group - Nitrobenzene - Nitroaromatic compound - Benzoyl - Chlorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Monosaccharide - Pyrimidine - Organosulfonic acid amide - Benzenoid - Sulfonyl - Aminosulfonyl compound - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Vinylogous amide - Oxolane - Urea - Secondary alcohol - 1,2-diol - Lactam - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organoheterocyclic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Oxacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Organohalogen compound - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic zwitterion - Organic oxide - Organic salt - Organic nitrogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteromonocyclic 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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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