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=FJWIHNJWTGEMPT-JZPVOVDPSA-N

C36H37NO5

563.694

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Glycosylamines N-alkylindoles 3-methylindoles Benzylethers Substituted pyrroles Oxanes Monosaccharides Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1-pyranosylindole - Glycosyl compound - N-glycosyl compound - 3-methylindole - N-alkylindole - 3-alkylindole - Benzylether - Indole - Indole or derivatives - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Substituted pyrrole - Oxane - Heteroaromatic compound - Pyrrole - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen 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