Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1OC([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NC(=O)NC1=CC=C(C=C1)S(=O)(=O)N1CCOCC1

InChIKey

InChIKey=OOHIOTPBUUPYRI-OFRRTHGGSA-N

Formula

C23H28N8O8S

Mass

576.59

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - Benzenesulfonamide - N-phenylurea - Benzenesulfonyl group - Imidazopyrimidine - Purine - Monocyclic benzene moiety - Morpholine - N-substituted imidazole - Oxazinane - Pyrimidine - Organosulfonic acid amide - Benzenoid - Imidolactam - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Imidazole - Heteroaromatic compound - Azole - Oxolane - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxamide group - Urea - Azacycle - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Organosulfur compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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