CCCCNC(=O)CC1=CN([C@@H]2O[C@H](COCC3=CC=CC=C3)[C@H](OCC3=CC=CC=C3)[C@H](OCC3=CC=CC=C3)[C@H]2O)C2=CC=CC=C12

InChIKey=YTNRZSQZDRWCNB-HXBMFNGISA-N

C41H46N2O6

662.827

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Glycosylamines 3-alkylindoles N-alkylindoles Benzylethers Substituted pyrroles Oxanes Monosaccharides Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Oxacyclic compounds Azacyclic compounds Dialkyl ethers Carbonyl compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1-pyranosylindole - N-glycosyl compound - Glycosyl compound - 3-alkylindole - N-alkylindole - Benzylether - Indole or derivatives - Indole - Oxane - Monosaccharide - Benzenoid - Monocyclic benzene moiety - Substituted pyrrole - Pyrrole - Heteroaromatic compound - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - 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