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Structure Information
Structure

Compound Identification

SMILES

NC1=NC(Br)=NC2=C1N=CN2[C@@H]1O[C@@]2(CO)CCO[C@H]2[C@H]1O

InChIKey

InChIKey=OWUDMTBGGMJOCE-BQIHAETKSA-N

Formula

C12H14BrN5O4

Mass

372.179

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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-aminopurine - Imidazopyrimidine - Purine - Furofuran - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - N-substituted imidazole - Monosaccharide - Aryl bromide - Aryl halide - Imidolactam - Pyrimidine - Imidazole - Azole - Heteroaromatic compound - Oxolane - Secondary alcohol - Oxacycle - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Primary amine - Organic oxygen compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organobromide - 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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