Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C2=C(C=C(F)C=C2)N=C1C1=CC=C(O1)[N+]([O-])=O

InChIKey

InChIKey=KUKKHHHRYXACTJ-PCBIJLKTSA-N

Formula

C16H14FN3O7

Mass

379.3

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Benzimidazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Benzimidazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-ribofuranosylbenzimidazole - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Benzimidazole - Nitroaromatic compound - 2-nitrofuran - Aryl fluoride - Aryl halide - Monosaccharide - N-substituted imidazole - Benzenoid - Azole - Furan - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Organic nitro compound - C-nitro compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Oxacycle - Organic oxoazanium - Azacycle - Primary alcohol - Organohalogen compound - Organofluoride - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organonitrogen compound - Organic zwitterion - Organic salt - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as benzimidazole ribonucleosides and ribonucleotides. These are nucleosides with a structure that consists of an imidazole moiety of benzimidazole is N-linked to a ribose (or deoxyribose). Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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