Structure Information
Structure

Compound Identification

SMILES

COC(=O)C(NC(=O)N1C(=O)C2(C(C3N(C2C2=CC=CC=C2OCCO)C(C(OC3=O)C2=CC=CC=C2)C2=CC=CC=C2)C(=O)NC2=NC3=CC=CC=C3S2)C2=CC=CC=C12)C(C)C

InChIKey

InChIKey=UXMXAQIDBKOCCV-UHFFFAOYSA-N

Formula

C49H45N5O9S

Mass

879.99

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Stilbenes

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Stilbenes

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Stilbene - N-carbamoyl-alpha-amino acid or derivatives - N-carbamoyl-alpha-amino acid - Valine or derivatives - Alpha-amino acid ester - Indolecarboxylic acid derivative - Phenylmorpholine - 2-phenylpyrrolidine - Alpha-amino acid or derivatives - Indole or derivatives - 1,3-benzothiazole - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-3-carboxamide - Phenol ether - N-arylamide - Phenoxy compound - Fatty acid ester - N-acyl urea - Aralkylamine - Alkyl aryl ether - Ureide - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Morpholine - Fatty acyl - Oxazinane - Benzenoid - N-alkylpyrrolidine - Methyl ester - Thiazole - Pyrrolidine - Pyrrole - Azole - Heteroaromatic compound - Dicarboximide - Tertiary amine - Amino acid or derivatives - Secondary carboxylic acid amide - Tertiary aliphatic amine - Carbonic acid derivative - Urea - Carboxamide group - Lactone - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Ether - Organic oxygen compound - Carbonyl group - Organic oxide - Alcohol - Organopnictogen compound - Primary alcohol - Amine - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Aromatic heteropolycyclic 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

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