Structure Information
Structure

Compound Identification

SMILES

CN(N=O)C(=O)NCCNC(=O)C1OC(C(O)C1O)N1C=NC2=C1NC=NC2=O

InChIKey

InChIKey=BKVPWJRKGBYYSU-UHFFFAOYSA-N

Formula

C14H18N8O7

Mass

410.347

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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-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - N-methylnitrosourea - Pyrimidone - N-substituted imidazole - Nitrosourea - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Nitrosamide - Vinylogous amide - Semicarbazide - Oxolane - Carboxamide group - 1,2-diol - Secondary carboxylic acid amide - Secondary alcohol - Organic n-nitroso compound - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitroso compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Alcohol - Organonitrogen compound - Organooxygen compound - Organic oxygen 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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