Structure Information
Structure

Compound Identification

SMILES

CO[C@H]1[C@@H](O)[C@H](CO)O[C@@H]1N1C=NC2=C1C=C(N)NC2=O

InChIKey

InChIKey=GBHXHNRNCTXLFX-RBHNIQJYSA-N

Formula

C12H16N4O5

Mass

296.283

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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 - Glycosyl compound - N-glycosyl compound - Imidazopyridinone - Imidazopyridine - Imidazo-[4,5-c]pyridine - Aminopyridine - Pyridinone - Monosaccharide - N-substituted imidazole - Pyridine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Secondary alcohol - Lactam - Organoheterocyclic compound - Dialkyl ether - Azacycle - Oxacycle - Ether - Alcohol - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Primary alcohol - Primary amine - Organooxygen compound - 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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