Structure Information
Structure

Compound Identification

SMILES

CC1=CC(\C=C(\CC[C@H]2OB(O)C[C@@H]3[C@H]4[C@@H](CC(CO)=C23)C(=O)N(CC2=CC=CS2)C4=O)C2=CC=CC=C2)=CC(C)=C1O

InChIKey

InChIKey=ZCAUDRQBBUDKJQ-IZSRPFHBSA-N

Formula

C34H36BNO6S

Mass

597.53

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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 - Isoindolone - Isoindoline - Isoindole or derivatives - Isoindole - O-cresol - Styrene - M-xylene - Xylene - Phenol - Monocyclic benzene moiety - 1,2-oxaborine derivative - Carboxylic acid imide, n-substituted - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Benzenoid - Boronic acid ester - Carboxylic acid imide - Thiophene - Pyrrolidine - Dicarboximide - Heteroaromatic compound - Boronic acid derivative - Lactam - Carboxylic acid derivative - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Alkylborane - Alcohol - Carbonyl group - Monoalkylborane - Primary alcohol - Organic metalloid moeity - Organonitrogen compound - Organooxygen 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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