Structure Information
Structure

Compound Identification

SMILES

NC1=CC2=C(N=CN2[C@H]2O[C@@H](CO)[C@H](O)[C@@H]2F)C(=O)N1

InChIKey

InChIKey=JXKJPSYTPBEHMA-BNTUSOOQSA-N

Formula

C11H13FN4O4

Mass

284.247

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Imidazole[4,5-c]pyridine ribonucleoside,ribonucleotide or analogue - Imidazopyridinone - Imidazopyridine - Imidazo-[4,5-c]pyridine - Aminopyridine - Pyridinone - N-substituted imidazole - Pyridine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Fluorohydrin - Halohydrin - Lactam - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Amine - Organohalogen compound - Organofluoride - Alkyl halide - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Alkyl fluoride - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as imidazole[4,5-c]pyridine ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole[4,5-c]pyridine ring system. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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