CC(=O)OCC1OC(C(OC(C)=O)C(OC(C)=O)C1OC(C)=O)N1CCC2=C1C=CC(=C2)[N+]([O-])=O

InChIKey=OYJPBOWPUKMYRC-UHFFFAOYSA-N

C22H26N2O11

494.453

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

1-pyranosylindoles

Not available

1-pyranosylindoles

Tetracarboxylic acids and derivatives Glycosylamines Indoles and derivatives Dialkylarylamines Nitroaromatic compounds Benzenoids Oxanes Monosaccharides Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Carbonyl compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides

Aromatic heteropolycyclic compounds

1-pyranosylindole - Tetracarboxylic acid or derivatives - Glycosyl compound - N-glycosyl compound - Indole or derivatives - Nitroaromatic compound - Dialkylarylamine - Monosaccharide - Oxane - Benzenoid - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Oxacycle - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - 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