Structure Information
Structure

Compound Identification

SMILES

[H]C1(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)OC([H])(N2C=NC3=C(O)NC(=N)C=C23)C([H])(O)C1([H])O

InChIKey

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