Compound Identification
SMILES
CCNC(=O)N1CCN(CC1)C1=CC=C(C=C1)C(=O)CCC1=CC=C(NC2=NCCN2)C=C1
InChIKey
InChIKey=FDGAWICRFLHDIV-UHFFFAOYSA-N
Formula
C25H32N6O2
Mass
448.571
Taxonomic Classification
Taxonomy Tree
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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 Retro-dihydrochalcones
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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
Retro-dihydrochalcones
Alternative Parents
Alkyl-phenylketones Phenylpiperazines N-arylpiperazines Butyrophenones Piperazine carboxamides Aniline and substituted anilines Aryl alkyl ketones Benzoyl derivatives Dialkylarylamines Imidazolines Ureas Guanidines Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Carboximidamides Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Retro-dihydrochalcone - Alkyl-phenylketone - N-arylpiperazine - Phenylpiperazine - Butyrophenone - Phenylketone - Piperazine-1-carboxamide - Tertiary aliphatic/aromatic amine - Benzoyl - Aryl ketone - Aryl alkyl ketone - Dialkylarylamine - Aniline or substituted anilines - Monocyclic benzene moiety - Benzenoid - Piperazine - 1,4-diazinane - 2-imidazoline - Guanidine - Ketone - Tertiary amine - Urea - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as retro-dihydrochalcones. These are a form of normal dihydrochalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
External Descriptors
Not available