CO[C@@H]1[C@@H](COCC2=CC=CC=C2)O[C@H]([C@H](OCC2=CC=CC=C2)[C@H]1OCC1=CC=CC=C1)N1C=C(C(=O)C(=O)OC)C2=CC=CC=C12

InChIKey=CDUJWMWDWDKGPX-MQPLVFOPSA-N

C39H39NO8

649.74

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Indole-3-acetic acid derivatives Glycosylamines N-alkylindoles Benzylethers Indoles Aryl ketones Alpha-keto acids and derivatives Substituted pyrroles Oxanes Monosaccharides Vinylogous amides Heteroaromatic compounds Methyl esters Oxacyclic compounds Dialkyl ethers Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Organonitrogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1-pyranosylindole - Indole-3-acetic acid derivative - Indolyl carboxylic acid derivative - Glycosyl compound - N-glycosyl compound - N-alkylindole - Indole or derivatives - Indole - Benzylether - Aryl ketone - Monocyclic benzene moiety - Alpha-keto acid - Benzenoid - Keto acid - Oxane - Monosaccharide - Substituted pyrrole - Heteroaromatic compound - Vinylogous amide - Methyl ester - Pyrrole - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organic oxygen 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