Compound Identification
SMILES
CSC1=CC=C(C=C2C(=O)N(C(=O)N(C2=O)C2=CC=C(C)C=C2)C2=CC=C(C)C=C2)C=C1
InChIKey
InChIKey=DYQOXWHJJNXQEA-UHFFFAOYSA-N
Formula
C26H22N2O3S
Mass
442.53
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Diazines
-
Subclass
Pyrimidines and pyrimidine derivatives
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Level 5
Pyrimidones
- Level 6 Barbituric acid derivatives
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Level 5
Pyrimidones
-
Subclass
Pyrimidines and pyrimidine derivatives
-
Class
Diazines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazines
Subclass
Pyrimidines and pyrimidine derivatives
Intermediate Tree Nodes
Pyrimidones
Direct Parent
Barbituric acid derivatives
Alternative Parents
Thiophenol ethers Toluenes N-acyl ureas Alkylarylthioethers Diazinanes Dicarboximides Sulfenyl compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Barbiturate - Aryl thioether - Thiophenol ether - N-acyl urea - Toluene - Ureide - Alkylarylthioether - 1,3-diazinane - Monocyclic benzene moiety - Benzenoid - Dicarboximide - Carbonic acid derivative - Urea - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Thioether - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as barbituric acid derivatives. These are compounds containing a perhydropyrimidine ring substituted at C-2, -4 and -6 by oxo groups.
External Descriptors
Not available