Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@@H](COCC2=CC=CC=C2)O[C@@H]([C@H](O)[C@H]1OCC1=CC=CC=C1)N1C=CC2=C1C(Cl)=CC=C2

InChIKey

InChIKey=XRCGBLRHZRSHQL-VNOXJOTMSA-N

Formula

C29H30ClNO5

Mass

508.01

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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 - Glycosyl compound - N-glycosyl compound - N-alkylindole - Benzylether - Indole or derivatives - Indole - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Substituted pyrrole - Oxane - Heteroaromatic compound - Pyrrole - Secondary alcohol - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - 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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