Structure Information
Structure

Compound Identification

SMILES

N[C@H](C(=O)OC[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)N1C=NC(=N1)C(N)=O)C1=CC=CC=C1

InChIKey

InChIKey=BBLBSXYFOBZRFK-VSBZFQJLSA-N

Formula

C16H19N5O6

Mass

377.357

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Triazole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Triazole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

N-ribosyl-1,2,4-triazole - Alpha-amino acid ester - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Pentose monosaccharide - 2-heteroaryl carboxamide - Aralkylamine - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Oxolane - 1,2,4-triazole - Triazole - Azole - Carboxylic acid ester - 1,2-diol - Amino acid or derivatives - Carboxamide group - Secondary alcohol - Primary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Organic nitrogen compound - Primary aliphatic amine - Organonitrogen compound - Carbonyl group - Organooxygen compound - Primary amine - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as triazole ribonucleosides and ribonucleotides. These are nucleoside derivatives containing a ribose (or deoxyribose) moiety which is N-glycosylated to a triazole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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