Compound Identification
SMILES
CCC(SC1=NC(=S)C2=CNN(C2=N1)C1=CC=CC=C1)C(N)=O
InChIKey
InChIKey=GJBAJAYKYHRULO-UHFFFAOYSA-N
Formula
C15H15N5OS2
Mass
345.44
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Imidazopyrimidines
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Subclass
Purines and purine derivatives
- Level 5 Dithioxanthines
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Subclass
Purines and purine derivatives
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Class
Imidazopyrimidines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Imidazopyrimidines
Subclass
Purines and purine derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Dithioxanthines
Alternative Parents
Phenylpyrazoles Pyrazolo[3,4-d]pyrimidines Pyrimidinethiones Alkylarylthioethers Fatty amides Benzene and substituted derivatives Heteroaromatic compounds Primary carboxylic acid amides Sulfenyl compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Dithioxanthine - Phenylpyrazole - Pyrazolo[3,4-d]pyrimidine - Pyrazolopyrimidine - Aryl thioether - Pyrimidinethione - Alkylarylthioether - Monocyclic benzene moiety - Fatty amide - Pyrimidine - Benzenoid - Fatty acyl - Heteroaromatic compound - Azole - Pyrazole - Carboxamide group - Primary carboxylic acid amide - Azacycle - Thioether - Sulfenyl compound - Carboxylic acid derivative - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as dithioxanthines. These are compounds containing a dithioxanthine moiety, a xanthine derivative obtained by replacing the two ketone groups by two thioketone groups.
External Descriptors
Not available