COC1=N[C@H](C(C)C)C(OC)=N[C@H]1CC1=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=CIAHEMXLOYZWQH-NWWMKSOSSA-N

C45H51N3O7

745.917

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Glycosylamines 3-alkylindoles N-alkylindoles Benzylethers Substituted pyrroles Imidolactones Monosaccharides Oxanes Heteroaromatic compounds Secondary alcohols Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organonitrogen compounds

Aromatic heteropolycyclic compounds

1-pyranosylindole - Glycosyl compound - N-glycosyl compound - N-alkylindole - 3-alkylindole - Benzylether - Indole - Indole or derivatives - Monocyclic benzene moiety - Imidolactone - Monosaccharide - Oxane - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Imido ester - Secondary alcohol - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Dialkyl ether - Propargyl-type 1,3-dipolar organic compound - 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