Compound Identification
SMILES
CCOC(=O)\C=C(/C)NC1=NC(=C(C)S1)C1=CC2=C(OC(=C(OC)C2=O)C2=CC=C(C)C=C2)C=C1
InChIKey
InChIKey=FXMMCSKUXCVCSB-DTQAZKPQSA-N
Formula
C27H26N2O5S
Mass
490.57
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Flavonoids
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Subclass
O-methylated flavonoids
- Level 5 3-O-methylated flavonoids
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Subclass
O-methylated flavonoids
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Class
Flavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Flavonoids
Subclass
O-methylated flavonoids
Intermediate Tree Nodes
Not available
Direct Parent
3-O-methylated flavonoids
Alternative Parents
Flavones 3-methoxychromones 2,4,5-trisubstituted thiazoles Toluenes Pyranones and derivatives Alkyl aryl ethers Fatty acid esters 2-amino-1,3-thiazoles Vinylogous amides Heteroaromatic compounds Enoate esters Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Enamines Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
3-methoxyflavonoid-skeleton - Flavone - 3-methoxychromone - Chromone - Benzopyran - 1-benzopyran - 2,4,5-trisubstituted 1,3-thiazole - Alkyl aryl ether - Fatty acid ester - Pyranone - Toluene - Monocyclic benzene moiety - 1,3-thiazol-2-amine - Fatty acyl - Benzenoid - Pyran - Azole - Enoate ester - Thiazole - Alpha,beta-unsaturated carboxylic ester - Vinylogous amide - Heteroaromatic compound - Carboxylic acid ester - Oxacycle - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Enamine - Ether - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxygen compound - Organic oxide - Amine - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 3-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C3 atom of the flavonoid backbone.
External Descriptors
Not available