OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)N1C=C(C(=O)C2=CN=CC=C2)C2=CC=CC=C12

InChIKey=UFRQOVZIQIBOMZ-XIKSMUEASA-N

C20H20N2O6

384.388

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Indolecarboxylic acids and derivatives Glycosylamines N-alkylindoles Pyridinecarboxylic acids and derivatives Indoles Aryl ketones Substituted pyrroles Benzenoids Oxanes Monosaccharides Vinylogous amides Heteroaromatic compounds 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Primary alcohols Organonitrogen compounds Organic oxides

Aromatic heteropolycyclic compounds

1-pyranosylindole - Indolecarboxylic acid derivative - Glycosyl compound - N-glycosyl compound - N-alkylindole - Indole - Pyridine carboxylic acid or derivatives - Indole or derivatives - Aryl ketone - Pyridine - Substituted pyrrole - Benzenoid - Oxane - Monosaccharide - Pyrrole - Heteroaromatic compound - Vinylogous amide - 1,2-diol - Ketone - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Polyol - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - 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