Structure Information
Structure

Compound Identification

SMILES

NC1=C(NC(=N1)[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)NCC1=CC=CC=C1

InChIKey

InChIKey=SWLCRSGCAIHELB-FOUMNBMASA-N

Formula

C16H20N4O5

Mass

348.359

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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 - Monocyclic benzene moiety - Monosaccharide - Imidolactam - Benzenoid - Azole - Heteroaromatic compound - Imidazole - Oxolane - Vinylogous amide - Amino acid or derivatives - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Carboxylic acid derivative - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic oxygen compound - Primary alcohol - Primary amine - Organonitrogen compound - Organooxygen 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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