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Structure Information
Structure

Compound Identification

SMILES

NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)S(=O)(=O)NCC(O)=O

InChIKey

InChIKey=ZJUYLSQUKZSWLE-KQYNXXCUSA-N

Formula

C10H16N4O8S

Mass

352.32

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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 - Alpha-amino acid or derivatives - Pentose monosaccharide - N-substituted imidazole - Monosaccharide - Aminoimidazole - Organosulfonic acid amide - Oxolane - Imidazole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Azole - Organosulfonic acid or derivatives - Amino acid or derivatives - 1,2-diol - Secondary alcohol - Amino acid - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic oxide - Amine - Organic oxygen compound - Alcohol - Carbonyl group - Organic nitrogen compound - Primary amine - Primary alcohol - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen 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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