Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=C(N)N=C(N1)C1(O[C@H](CO)[C@@H](O)[C@H]1O)C1=NC(N)=C(N1)C(N)=O

InChIKey

InChIKey=QVKHSQWQMBNQSL-BZSWDTDFSA-N

Formula

C13H18N8O6

Mass

382.337

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

C2-linked imidazole ribonucleosides and ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

C2-linked imidazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

C2-linked imidazole ribonucleoside - C-glycosyl compound - Glycosyl compound - Pentose monosaccharide - 2-heteroaryl carboxamide - 2,4,5-trisubstituted-imidazole - Trisubstituted imidazole - Imidazole-4-carbonyl group - Aminoimidazole - Monosaccharide - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Oxolane - Vinylogous amide - Amino acid or derivatives - Secondary alcohol - Primary carboxylic acid amide - 1,2-diol - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Primary alcohol - Amine - Primary amine - Organic nitrogen compound - Alcohol - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as c2-linked imidazole ribonucleosides and ribonucleotides. These are nucleoside and nucleotide analogues with a structure that consists of an imidazole ring system which is substituted at the C2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.

External Descriptors

Not available

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