Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)C1OC(C(O)C1O)N1C=NC2=C1N=C(N=C2N)C#CC1=CC=CC=C1C=O

InChIKey

InChIKey=YVVWPOITEWGFTD-UHFFFAOYSA-N

Formula

C21H20N6O5

Mass

436.428

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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-aminopurine - Imidazopyrimidine - Purine - Benzaldehyde - Benzoyl - Aminopyrimidine - Aryl-aldehyde - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Carboxamide group - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Alcohol - Aldehyde - Organooxygen compound - Primary amine - 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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