COC(=O)N\N=C\C1=C(Cl)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C2=CC(Cl)=C(Cl)C=C12

InChIKey=MXTKNBDNTCUQMV-MFHRDMSVSA-N

C16H16Cl3N3O6

452.67

Organic compounds

Nucleosides, nucleotides, and analogues

Indole ribonucleosides and ribonucleotides

Not available

Not available

Indole ribonucleosides and ribonucleotides

Glycosylamines Pentoses N-alkylindoles Indoles Substituted pyrroles Aryl chlorides Benzenoids Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organochlorides Carbonyl compounds Organonitrogen compounds Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - N-alkylindole - Indole - Indole or derivatives - Benzenoid - Substituted pyrrole - Aryl chloride - Aryl halide - Monosaccharide - Heteroaromatic compound - Pyrrole - Oxolane - Secondary alcohol - 1,2-diol - Azacycle - Organoheterocyclic compound - Oxacycle - Hydrocarbon derivative - Organohalogen compound - Organochloride - Alcohol - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organic oxide - Primary alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as indole ribonucleosides and ribonucleotides. These are compounds in which the C-1 of a ribosyl (or deoxyribosyl) moiety is linked to the N1-position of an indole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

Not available