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Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@H](O[N+]([O-])=O)[C@@H]1O[N+]([O-])=O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=CHMXERRSDPKARP-BSFVXNEUSA-N

Formula

C12H14N8O8

Mass

398.292

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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 - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Alkyl nitrate - Azole - Imidazole - Heteroaromatic compound - Organic nitrate - Oxolane - Organic nitro compound - Amino acid or derivatives - Carboxamide group - Organic nitric acid or derivatives - Secondary carboxylic acid amide - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Organic oxygen compound - Carbonyl group - Organic salt - Primary amine - Organonitrogen compound - Organooxygen 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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