Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OCC1OC(C(OC=O)C1OC=O)N1C=NC2=C1N=CN=C2NC=O

InChIKey

InChIKey=MDJJWKIMHFERMP-UHFFFAOYSA-N

Formula

C20H19N5O9S

Mass

505.46

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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 - Benzenesulfonate ester - P-methylbenzenesulfonate - N-glycosyl compound - Glycosyl compound - Tosyl compound - Benzenesulfonate - Benzenesulfonyl group - Purine - Imidazopyrimidine - Arylsulfonic acid or derivatives - N-arylamide - Toluene - Imidolactam - Benzenoid - Organosulfonic acid ester - Pyrimidine - N-substituted imidazole - Monosaccharide - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Heteroaromatic compound - Tetrahydrofuran - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Imidazole - Azole - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - 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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