Structure Information
Structure

Compound Identification

SMILES

CS(=O)(=O)C1=CC=C(CNC2=NC=NC3=C2N=CN3[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2NC(=O)COC2=CC=CC=C2)C=C1

InChIKey

InChIKey=ZOASNWKJCPXWJF-PAGNRNNLSA-N

Formula

C26H28N6O7S

Mass

568.61

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Benzenesulfonyl group - Imidazopyrimidine - Purine - Phenoxy compound - Benzylamine - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Sulfonyl - Sulfone - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary carboxylic acid amide - Carboxamide group - Secondary alcohol - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Ether - Amine - Organic oxide - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organosulfur compound - Organooxygen compound - Primary alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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