Structure Information
Structure

Compound Identification

SMILES

CN1C=NC(=C1SC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)[N+]([O-])=O

InChIKey

InChIKey=YGMZALSIUBISJA-HTVVRFAVSA-N

Formula

C14H15N7O6S

Mass

409.38

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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 - Diarylthioether - 6-thiopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Aryl thioether - Nitroaromatic compound - Nitroimidazole - Pyrimidine - Monosaccharide - N-substituted imidazole - Imidolactam - Azole - Imidazole - Oxolane - Heteroaromatic compound - 1,2-diol - Organic nitro compound - C-nitro compound - Secondary alcohol - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Organic 1,3-dipolar compound - Thioether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxoazanium - Primary alcohol - Organonitrogen compound - Alcohol - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic zwitterion - Organic nitrogen compound - Organic salt - 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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