Compound Identification
SMILES
CCCC1(CCC)NC(=O)N(CC2=C3CCC(CC3OC(O)=C2)=NC(C)=O)C1=O
InChIKey
InChIKey=FZTRVHOULOYVJZ-UHFFFAOYSA-N
Formula
C21H29N3O5
Mass
403.479
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Azolidines
-
Subclass
Imidazolidines
-
Level 5
Imidazolidinones
-
Level 6
Imidazolidinediones
- Level 7 Hydantoins
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Level 6
Imidazolidinediones
-
Level 5
Imidazolidinones
-
Subclass
Imidazolidines
-
Class
Azolidines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Azolidines
Subclass
Imidazolidines
Intermediate Tree Nodes
Imidazolidinones - Imidazolidinediones
Direct Parent
Hydantoins
Alternative Parents
Alpha amino acids and derivatives Ureides Pyrans Secondary ketimines Dicarboximides Azomethines N-acylimines Ketene acetals Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Hydantoin - Alpha-amino acid or derivatives - Ureide - Pyran - Azomethine - Dicarboximide - Secondary ketimine - Ketene acetal or derivatives - Urea - N-acylimine - Azacycle - Oxacycle - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as hydantoins. These are heterocyclic compounds containing an imidazolidine substituted by ketone group at positions 2 and 4.
External Descriptors
Not available