Structure Information
Structure

Compound Identification

SMILES

CC(=O)OCC1OC(C(OC(C)=O)C1OC(C)=O)N1C=NC(=C1Br)[N+]([O-])=O

InChIKey

InChIKey=KWZVMAYKLHVMRZ-UHFFFAOYSA-N

Formula

C14H16BrN3O9

Mass

450.198

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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 - N-glycosyl compound - Glycosyl compound - Tricarboxylic acid or derivatives - Nitroaromatic compound - Nitroimidazole - Imidolactam - N-substituted imidazole - Monosaccharide - Aryl halide - Aryl bromide - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Organic nitro compound - C-nitro compound - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Carbonyl group - 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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