Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=NN(C=N1)[C@@H]1O[C@H](COC(=O)CNC(=O)C2=CC=CC=C2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=YKEHZZNHTNAYMU-CNEMSGBDSA-N

Formula

C17H19N5O7

Mass

405.367

Export to:

JSON SDF CSV

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 - N-acyl-alpha amino acid or derivatives - Hippuric acid or derivatives - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Pentose monosaccharide - Benzamide - Benzoic acid or derivatives - 2-heteroaryl carboxamide - Benzoyl - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Azole - Heteroaromatic compound - Oxolane - 1,2,4-triazole - Triazole - 1,2-diol - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Secondary alcohol - Primary carboxylic acid amide - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - 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

Previous Back Next