Compound Identification
SMILES
COC1=CC=CC2=C1C1=C(C=C(NS(C)(=O)=O)C=C1)C(O2)C1=CC=CC(\C=C\C2=CC=CC=C2)=C1
InChIKey
InChIKey=NNWINEPPWGUFBB-CCEZHUSRSA-N
Formula
C29H25NO4S
Mass
483.58
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Flavonoids
-
Subclass
O-methylated flavonoids
- Level 5 5-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
5-O-methylated flavonoids
Alternative Parents
Stilbenes Dibenzopyrans Sulfanilides 2-benzopyrans Styrenes Anisoles Alkyl aryl ethers Organosulfonamides Organic sulfonamides Aminosulfonyl compounds Oxacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
5-methoxyflavonoid-skeleton - Dibenzopyran - Stilbene - Benzopyran - 2-benzopyran - 1-benzopyran - Sulfanilide - Anisole - Phenol ether - Styrene - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid amide - Organic sulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Ether - Organoheterocyclic compound - Oxacycle - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.
External Descriptors
Not available