Structure Information
Structure

Compound Identification

SMILES

CN(C(=O)[C@H]1C[C@H](C=C1)N1C=NC2=C1N=C(N=C2Cl)N(C=O)C(=O)OC(C)(C)C)S(=O)(=O)C1=CC=CC=C1[N+]([O-])=O

InChIKey

InChIKey=SNWACFREXOZCRQ-CABCVRRESA-N

Formula

C24H24ClN7O8S

Mass

606.01

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Nucleoside and nucleotide analogues

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Benzenesulfonamide - Imidazopyrimidine - Benzenesulfonyl group - Nitrobenzene - Purine - Nitroaromatic compound - Halopyrimidine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Benzenoid - Azole - Imidazole - Dicarboximide - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Carbamic acid ester - Aminosulfonyl compound - C-nitro compound - Organic nitro compound - Organoheterocyclic compound - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Azacycle - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organic oxygen compound - Organochloride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.

External Descriptors

Not available

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