Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=GWDGDCJMRNUKEW-MGUDNFKCSA-N

Formula

C11H17N4O14P3

Mass

522.192

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