NC(=S)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=GCIFOKRAPOLNOS-IMWZBCAKSA-N

C15H15Cl3N4O4S

453.72

Organic compounds

Nucleosides, nucleotides, and analogues

Indole ribonucleosides and ribonucleotides

Not available

Not available

Indole ribonucleosides and ribonucleotides

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

Aromatic heteropolycyclic compounds

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