Structure Information
Structure

Compound Identification

SMILES

COC(=O)CC1=C(N=NN1[C@@H]1O[C@H](COC(=O)C2=CC=CC=C2)[C@@H](OC(=O)C2=CC=CC=C2)[C@H]1OC(=O)C1=CC=CC=C1)C(=O)OC

InChIKey

InChIKey=AXSUHJNCKRBXRU-BSULFMODSA-N

Formula

C33H29N3O11

Mass

643.605

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-1,2,3-triazole - N-glycosyl compound - Glycosyl compound - Benzoate ester - Pentose monosaccharide - Benzoic acid or derivatives - Benzoyl - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Azole - Vinylogous amide - Methyl ester - 1,2,3-triazole - Oxolane - Heteroaromatic compound - Carboxylic acid ester - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - 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