Structure Information
Structure

Compound Identification

SMILES

COCCNC(=O)[C@H]1O[C@H]([C@@H]2OC(C)(C)O[C@H]12)N1C=NC2=C1N=CN=C2NCCC1=CN(CC2=CC=C(Cl)C=C2)C2=CC=CC=C12

InChIKey

InChIKey=KALZDXRURYZHFE-FFAHVWSXSA-N

Formula

C33H36ClN7O5

Mass

646.15

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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 - 6-alkylaminopurine - 6-aminopurine - N-alkylindole - 3-alkylindole - Imidazopyrimidine - Indole - Indole or derivatives - Purine - Aminopyrimidine - Chlorobenzene - Ketal - Halobenzene - Secondary aliphatic/aromatic amine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - N-substituted imidazole - Pyrimidine - Imidolactam - Substituted pyrrole - Benzenoid - Oxolane - Azole - Meta-dioxolane - Pyrrole - Imidazole - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organic nitrogen compound - Organochloride - Organopnictogen compound - Organohalogen compound - Organic oxide - Organooxygen compound - Hydrocarbon derivative - 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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