Structure Information
Structure

Compound Identification

SMILES

CC1(C)O[C@@H]2[C@H](O1)[C@H](O[C@H]2N1C=NC2=C1N=CN=C2NCCC1=CN(CCN2CCCC2)C2=CC=CC=C12)C(=O)NC1CC1

InChIKey

InChIKey=UANMGXXAQWLHLF-KUYWTNKVSA-N

Formula

C32H40N8O4

Mass

600.724

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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 - 3-alkylindole - N-alkylindole - Indole or derivatives - Purine - Indole - Imidazopyrimidine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Ketal - N-alkylpyrrolidine - N-substituted imidazole - Pyrimidine - Imidolactam - Benzenoid - Substituted pyrrole - Meta-dioxolane - Azole - Imidazole - Heteroaromatic compound - Oxolane - Pyrrole - Pyrrolidine - Tertiary amine - Amino acid or derivatives - Secondary carboxylic acid amide - Tertiary aliphatic amine - Carboxamide group - Oxacycle - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Acetal - Amine - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - 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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