NC1=NC(=O)C2=C(N1)N([C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C(=N2)C#CC1=CC=C(CC(=O)C2=CC=CC=C2)C=C1

InChIKey=LSEVAWOVGCIVFH-PXOHRUDZSA-N

C26H23N5O6

501.499

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Stilbene glycosides

Not available

Stilbene glycosides

Purine nucleosides Alkyl-phenylketones Glycosylamines 6-oxopurines Pentoses Hypoxanthines Aryl alkyl ketones Benzoyl derivatives Pyrimidones Aminopyrimidines and derivatives N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives Primary alcohols

Aromatic heteropolycyclic compounds

Stilbene glycoside - Purine nucleoside - Alkyl-phenylketone - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Pentose monosaccharide - Hypoxanthine - Purinone - Phenylketone - Imidazopyrimidine - Purine - Benzoyl - Aryl alkyl ketone - Aryl ketone - Aminopyrimidine - Pyrimidone - Pyrimidine - Benzenoid - Monosaccharide - Monocyclic benzene moiety - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - Secondary alcohol - 1,2-diol - Ketone - Organoheterocyclic compound - Oxacycle - Azacycle - Primary alcohol - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Primary amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as stilbene glycosides. These are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

Not available