Structure Information
Structure

Compound Identification

SMILES

COC1=C(C=C(Cl)C=C1)C1(F)C(=O)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=C1C=CC(=C2)C(F)(F)F

InChIKey

InChIKey=RLYOCPULACVNHH-FTLKZCOISA-N

Formula

C22H20ClF4NO7

Mass

521.85

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

1-pyranosylindoles

Intermediate Tree Nodes

Not available

Direct Parent

1-pyranosylindoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-pyranosylindole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Indole or derivatives - Anisole - Phenoxy compound - Phenol ether - Methoxybenzene - Chlorobenzene - Alkyl aryl ether - Halobenzene - Aryl chloride - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Oxane - Aryl halide - Tertiary carboxylic acid amide - Carboxamide group - Secondary alcohol - Lactam - Oxacycle - Carboxylic acid derivative - Azacycle - Polyol - Ether - Organoheterocyclic compound - Organofluoride - Organic nitrogen compound - Primary alcohol - Organooxygen compound - Alkyl fluoride - Alcohol - Carbonyl group - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1-pyranosylindoles. These are nucleoside and nucleotide analogs with a structure that consists of an indole base which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.

External Descriptors

Not available

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