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Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC(=C1)[C@H](O)[C@@H](Cl)CN=[N+]=[N-]

InChIKey

InChIKey=JCXNFWNGFYOMAA-UVNHIURDSA-N

Formula

C11H16ClN5O5

Mass

333.73

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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 - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - N-substituted imidazole - Monosaccharide - Imidazole - Heteroaromatic compound - Oxolane - Azole - 1,2-diol - Azo compound - Azo imide - Secondary alcohol - Chlorohydrin - Halohydrin - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic alcohol - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxygen compound - Alkyl halide - Alkyl chloride - Alcohol - 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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