COC(=O)CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=CC=CC=C12

InChIKey=UCJQLVSIHYDTNQ-USACIQFYSA-N

C17H21NO7

351.355

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Indole-3-acetic acid derivatives Hexoses Glycosylamines 3-alkylindoles N-alkylindoles Substituted pyrroles Benzenoids Oxanes Heteroaromatic compounds Methyl esters 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Organonitrogen compounds Carbonyl compounds Primary alcohols

Aromatic heteropolycyclic compounds

1-pyranosylindole - Indole-3-acetic acid derivative - Indolyl carboxylic acid derivative - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - N-alkylindole - 3-alkylindole - Indole - Indole or derivatives - Monosaccharide - Benzenoid - Substituted pyrrole - Oxane - Methyl ester - Pyrrole - Heteroaromatic compound - Carboxylic acid ester - Secondary alcohol - 1,2-diol - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Primary alcohol - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

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.

Not available