Compound Identification
SMILES
[Na+].O[C@H]([C@@H](NCC([O-])=O)C1=CC=CC=C1)C1=CC=CC=C1
InChIKey
InChIKey=ZXWPCMCFUFTJRS-MOGJOVFKSA-M
Formula
C16H16NNaO3
Mass
293.298
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Stilbenes
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Stilbenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Stilbenes
Alternative Parents
Alpha amino acids Aralkylamines Benzene and substituted derivatives Secondary alcohols 1,2-aminoalcohols Amino acids Carboxylic acid salts Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Carbonyl compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides Organic sodium salts Organic zwitterions
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Stilbene - Alpha-amino acid - Alpha-amino acid or derivatives - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Secondary alcohol - 1,2-aminoalcohol - Carboxylic acid salt - Amino acid - Amino acid or derivatives - Carboxylic acid - Monocarboxylic acid or derivatives - Secondary amine - Carboxylic acid derivative - Secondary aliphatic amine - Organic alkali metal salt - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic alcohol - Organic zwitterion - Organic salt - Carbonyl group - Organic sodium salt - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Alcohol - Aromatic homomonocyclic compound
Description
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.
External Descriptors
Not available