Structure Information
Structure

Compound Identification

SMILES

OCC1OC(C(O)C1O)N1C=NC2=C(CC3=CC=C(C=C3)[N+]([O-])=O)N=CN=C12

InChIKey

InChIKey=JDVXMOKFIDYPPV-UHFFFAOYSA-N

Formula

C17H17N5O6

Mass

387.352

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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 - Pentose monosaccharide - Imidazopyrimidine - Nitrobenzene - Purine - Nitroaromatic compound - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Imidazole - Azole - Oxolane - Heteroaromatic compound - Organic nitro compound - Secondary alcohol - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Azacycle - Oxacycle - Alcohol - Organic zwitterion - Organic oxide - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Primary 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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