Structure Information
Structure

Compound Identification

SMILES

O[13CH2][C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC=C1[N+]([O-])=O

InChIKey

InChIKey=MNKZJKGAWFXTBY-VBYAISPESA-N

Formula

C8H11N3O6

Mass

246.183

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Imidazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Imidazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Imidazole ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Nitroaromatic compound - Nitroimidazole - Monosaccharide - N-substituted imidazole - Azole - Imidazole - Heteroaromatic compound - Oxolane - C-nitro compound - Organic nitro compound - Secondary alcohol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Oxacycle - Organoheterocyclic compound - Azacycle - Organic oxoazanium - Organic zwitterion - Organonitrogen compound - Alcohol - Organooxygen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organic nitrogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as imidazole ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. This class does not contain benzimidazole nucleosides and nucleotides.

External Descriptors

Not available

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