Structure Information
Structure

Compound Identification

SMILES

NC1=NC=CC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=UJWQFZLUZREXBH-PNHWDRBUSA-N

Formula

C11H17N4O13P3

Mass

506.193

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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 - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyridine - Imidazo-[4,5-c]pyridine - Monoalkyl phosphate - Aminopyridine - Imidolactam - Monosaccharide - Alkyl phosphate - N-substituted imidazole - Pyridine - Organic phosphoric acid derivative - Phosphoric acid ester - Imidazole - Heteroaromatic compound - Oxolane - Azole - 1,2-diol - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Alcohol - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Hydrocarbon derivative - Amine - 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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