CN1C=C(C2=CC=CC=C12)C1=C(C(=O)NC1=O)C1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=CC=CC=C12

InChIKey=UBWJYONKCBPKDX-GNAGPYCMSA-N

C27H25N3O7

503.511

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Hexoses Glycosylamines N-alkylindoles Indoles Maleimides N-methylpyrroles Oxanes Benzenoids N-unsubstituted carboxylic acid imides Pyrrolines Heteroaromatic compounds Dicarboximides 1,2-diols Secondary alcohols Azacyclic compounds Oxacyclic compounds Organonitrogen compounds Organic oxides Primary alcohols Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

1-pyranosylindole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - N-alkylindole - Indole or derivatives - Indole - Maleimide - N-methylpyrrole - Oxane - Monosaccharide - Benzenoid - Substituted pyrrole - Carboxylic acid imide, n-unsubstituted - Carboxylic acid imide - Pyrroline - Pyrrole - Heteroaromatic compound - Dicarboximide - 1,2-diol - Secondary alcohol - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Primary alcohol - Organic nitrogen 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