Compound Identification
SMILES
CCN1CCN(CC1)C(=O)CC(=O)CN1CC2CC(C1)C1=CC=CC(=O)N1C2
InChIKey
InChIKey=LTTMJUKQFRQYPU-UHFFFAOYSA-N
Formula
C21H30N4O3
Mass
386.496
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
-
Class
Lupin alkaloids
- Subclass Cytisine and derivatives
-
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
Pyridinones N-alkylpiperazines Aralkylamines Piperidines 1,3-dicarbonyl compounds Tertiary carboxylic acid amides Heteroaromatic compounds Alpha-amino ketones Trialkylamines Lactams Amino acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cytisine - Pyridinone - N-alkylpiperazine - Aralkylamine - 1,4-diazinane - Piperazine - Piperidine - Pyridine - 1,3-dicarbonyl compound - Heteroaromatic compound - Alpha-aminoketone - Tertiary carboxylic acid amide - Carboxamide group - Tertiary aliphatic amine - Ketone - Lactam - Amino acid or derivatives - Tertiary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Amine - Organic oxide - Organic oxygen compound - Carbonyl group - 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