Structure Information
Structure

Compound Identification

SMILES

NC(=O)C1=NN(C=N1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.COC1=C(C=CC(NC(=O)NN(CC2=CC=CC=C2)C(=O)O[C@H]2CCOC2)=C1)C1=CN=CO1

InChIKey

InChIKey=XDLQWALZVHUDGM-ZUFLITNJSA-N

Formula

C31H36N8O11

Mass

696.674

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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

Not available

Substituents

N-ribosyl-1,2,4-triazole - Phenyl-1,3-oxazole - N-glycosyl compound - Glycosyl compound - N-phenylurea - Methoxyaniline - 2-heteroaryl carboxamide - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Azole - Oxazole - Oxolane - Heteroaromatic compound - 1,2,4-triazole - Triazole - Semicarbazide - Secondary alcohol - 1,2-diol - Carboxamide group - Primary carboxylic acid amide - Oxacycle - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Organic oxygen compound - Alcohol - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - 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

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