Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@H](O)[C@H](OC1N1C=NC2=C1N=CN=C2NCCC1=CN(CCN2CCOCC2)C2=CC=CC=C12)C(=O)NC1CC1

InChIKey

InChIKey=ZFQSSPPDZXAZRM-JVPDDODCSA-N

Formula

C29H36N8O5

Mass

576.658

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