Structure Information
Structure

Compound Identification

SMILES

ClC1=NC(NC=O)=NC2=C1N=CN2C1OC(COCC2=CC=CC=C2)C(OCC2=CC=CC=C2)C1OCC1=CC=CC=C1

InChIKey

InChIKey=LUVHHLQYQUVEDJ-UHFFFAOYSA-N

Formula

C32H30ClN5O5

Mass

600.07

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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 - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Imidazopyrimidine - Purine - Benzylether - N-arylamide - Halopyrimidine - Benzenoid - N-substituted imidazole - Pyrimidine - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - Azole - Imidazole - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - 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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