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Structure Information
Structure

Compound Identification

SMILES

NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C1=C(Br)C=NN1

InChIKey

InChIKey=XAWHFLAKBYKTCP-MGUDNFKCSA-N

Formula

C11H14BrN5O4

Mass

360.168

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Imidazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Imidazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Imidazole ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminoimidazole - Aryl bromide - Aryl halide - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Pyrazole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Amine - Organohalogen compound - Organobromide - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Primary alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as imidazole ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. This class does not contain benzimidazole nucleosides and nucleotides.

External Descriptors

Not available

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