CO[C@@H]1[C@@H](COCC2=CC=CC=C2)O[C@@H]([C@H](O)[C@H]1OCC1=CC=CC=C1)N1C=C(CC(N)=O)C2=C1C(Cl)=CC=C2

InChIKey=ZDIVIGIYRBCRHH-FCLMYRLYSA-N

C31H33ClN2O6

565.06

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 Aryl chlorides Monosaccharides Heteroaromatic compounds Secondary alcohols Primary carboxylic acid amides Oxacyclic compounds Azacyclic compounds Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides Organonitrogen compounds

Aromatic heteropolycyclic compounds

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