Compound Identification
SMILES
CC(C)(C1=CC=C(OC2=CC3=C(C=C2)C(=O)N(C3=O)C2=CC=C(C=CC(=O)C3=CC=CC=C3)C=C2)C=C1)C1=CC=C(OC2=CC3=C(C=C2)C(=O)N(C3=O)C2=CC=C(C=CC(=O)C3=CC=CC=C3)C=C2)C=C1
InChIKey
InChIKey=GDCPICLWNGXITL-UHFFFAOYSA-N
Formula
C61H42N2O8
Mass
931.013
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
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Class
Linear 1,3-diarylpropanoids
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Subclass
Chalcones and dihydrochalcones
- Level 5 Retrochalcones
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Subclass
Chalcones and dihydrochalcones
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Class
Linear 1,3-diarylpropanoids
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Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Linear 1,3-diarylpropanoids
Subclass
Chalcones and dihydrochalcones
Intermediate Tree Nodes
Not available
Direct Parent
Retrochalcones
Alternative Parents
Diphenylmethanes Cinnamic acids and derivatives Phthalimides Diarylethers Phenylpropanes Isoindoles Aryl ketones Phenoxy compounds Styrenes Benzoyl derivatives Phenol ethers N-substituted carboxylic acid imides Enones Acryloyl compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Retrochalcone - Diphenylmethane - Cinnamic acid or derivatives - Phthalimide - Diaryl ether - Isoindolone - Isoindole or derivatives - Phenylpropane - Isoindole - Isoindoline - Phenoxy compound - Styrene - Aryl ketone - Phenol ether - Benzoyl - Benzenoid - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Acryloyl-group - Carboxylic acid imide - Enone - Alpha,beta-unsaturated ketone - Ketone - Organoheterocyclic compound - Ether - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
External Descriptors
Not available