Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCC1=CC=CC=C1Br

InChIKey

InChIKey=GISWABNYIIDLSG-LSCFUAHRSA-N

Formula

C17H18BrN5O4

Mass

436.266

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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 - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Benzylamine - Aminopyrimidine - Halobenzene - Bromobenzene - Aryl bromide - Monosaccharide - N-substituted imidazole - Aryl halide - Pyrimidine - Benzenoid - Imidolactam - Monocyclic benzene moiety - Heteroaromatic compound - Imidazole - Azole - Oxolane - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organobromide - Organonitrogen compound - Organooxygen compound - Primary alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Alcohol - Organohalogen 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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