Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC(CNC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC(=N2)C(N)=O)=C1OCC1=C(Cl)C=C(F)C=C1

InChIKey

InChIKey=FVDOVVMOIORDJV-FZONSQQESA-N

Formula

C23H25ClFN5O6

Mass

521.93

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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 - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 2-heteroaryl carboxamide - Phenoxy compound - Anisole - Benzylamine - Methoxybenzene - Phenol ether - Phenylmethylamine - Alkyl aryl ether - Chlorobenzene - Fluorobenzene - Aralkylamine - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Oxolane - Triazole - 1,2,4-triazole - Azole - Heteroaromatic compound - Secondary alcohol - Primary carboxylic acid amide - 1,2-diol - Amino acid or derivatives - Carboxamide group - Secondary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Secondary aliphatic amine - Ether - Oxacycle - Amine - Organooxygen compound - Organic nitrogen compound - Alcohol - Organohalogen compound - Organic oxide - Organonitrogen compound - Organofluoride - Hydrocarbon derivative - Organochloride - Organic oxygen 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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