CC1(C)C2CC[C@@]1(CS([O-])(=O)=O)C(=O)C2.CC([NH3+])C(O)(CC1=CC=CC=C1)C1=CC=CC=C1

InChIKey=VONVNOMDXZAJFC-FHIDHQGESA-N

C26H35NO5S

473.63

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Amphetamines and derivatives Aromatic monoterpenoids Bicyclic monoterpenoids Phenylpropanes Aralkylamines Tertiary alcohols Sulfonyls Quaternary ammonium salts Organosulfonic acids Alkanesulfonic acids 1,2-aminoalcohols Ketones Hydrocarbon derivatives Aromatic alcohols Monoalkylamines Organic oxides Organic zwitterions Organopnictogen compounds

Not available

Stilbene - Amphetamine or derivatives - Aromatic monoterpenoid - Bornane monoterpenoid - Norbornane monoterpenoid - Bicyclic monoterpenoid - Monoterpenoid - Phenylpropane - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Alkanesulfonic acid - Quaternary ammonium salt - Tertiary alcohol - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Ketone - 1,2-aminoalcohol - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Aromatic alcohol - Carbonyl group - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Alcohol - Aromatic homopolycyclic compound

This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Not available