Compound Identification
SMILES
CCCCC1=CC=C(NC(=O)C(NC(=O)N2CC3CC(C2)C2=CC=CC(=O)N2C3)C(C)C)C=C1
InChIKey
InChIKey=YFFWUDLNTSJFKM-UHFFFAOYSA-N
Formula
C27H36N4O3
Mass
464.61
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Cytisine and derivatives
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Class
Lupin alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Lupin alkaloids
Subclass
Cytisine and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Cytisine and derivatives
Alternative Parents
Valine and derivatives N-carbamoyl-alpha amino acids and derivatives Alpha amino acid amides Anilides Piperidinecarboxamides N-arylamides Pyridinones Fatty amides Heteroaromatic compounds Ureas Lactams Secondary carboxylic acid amides Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cytisine - Valine or derivatives - N-carbamoyl-alpha-amino acid or derivatives - Alpha-amino acid amide - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - 1-piperidinecarboxamide - Piperidinecarboxamide - Anilide - N-arylamide - Pyridinone - Monocyclic benzene moiety - Fatty amide - Piperidine - Pyridine - Fatty acyl - Benzenoid - Heteroaromatic compound - Urea - Secondary carboxylic acid amide - Carbonic acid derivative - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as cytisine and derivatives. These are lupin alkaloids with a structure based on the cytisine skeleton, which is a tetracyclic ketone containing fused pyridine and piperidine rings that form pyrido[1,2a][1,5]diazocin-8-one.
External Descriptors
Not available