Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@H](O)[C@H](O[C@H]1N1C=NC2=C1N=CN=C2NCCC1=CN(CCN2CCCCC2)C2=CC=CC=C12)C(=O)NC1CC1

InChIKey

InChIKey=LQFAEGMDAWKIMD-YRIIQKNPSA-N

Formula

C30H38N8O4

Mass

574.686

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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 - 6-alkylaminopurine - N-alkylindole - 6-aminopurine - 3-alkylindole - Purine - Indole or derivatives - Indole - Imidazopyrimidine - Aminopyrimidine - Piperidine - Pyrimidine - N-substituted imidazole - Substituted pyrrole - Imidolactam - Benzenoid - Azole - Oxolane - Pyrrole - Heteroaromatic compound - Imidazole - Amino acid or derivatives - Carboxamide group - 1,2-diol - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Amine - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen 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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