Compound Identification
SMILES
CN(C)[C@@H](C(=O)N1CCC[C@H]1C1=NC=C(C1)C1=CC=C(C=C1)C(=O)CC1=CC=C(C=C1)C1=CN=C(N1)[C@@H]1CCCN1C(=O)[C@H](N(C)C)C1=CC=CC=C1)C1=CC=CC=C1
InChIKey
InChIKey=YRNIVFRLWSGNIE-PVIZNTCDSA-N
Formula
C49H53N7O3
Mass
788.009
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
Alkyl-phenylketones Phenylimidazoles Alpha amino acids and derivatives Phenylacetamides N-acylpyrrolidines Aryl alkyl ketones Benzoyl derivatives Aralkylamines Tertiary carboxylic acid amides Heteroaromatic compounds Trialkylamines Ketimines Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Stilbene - Alkyl-phenylketone - 5-phenylimidazole - 4-phenylimidazole - Alpha-amino acid or derivatives - Phenylacetamide - Phenylketone - Benzoyl - N-acylpyrrolidine - Aryl alkyl ketone - Aryl ketone - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Pyrrolidine - Tertiary carboxylic acid amide - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Ketone - Ketimine - Carboxamide group - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organooxygen compound - Amine - Imine - Carbonyl group - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Aromatic heteromonocyclic 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