Compound Identification
SMILES
CN(C)C1=CC=C(CNC2=CC=C3[C@@H]4C[C@@H](CN(C4)C(=O)NC4CCCCC4)CN3C2=O)C=C1
InChIKey
InChIKey=QFXVHIIZMMTAKU-LEWJYISDSA-N
Formula
C27H37N5O2
Mass
463.626
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
Piperidinecarboxamides Aniline and substituted anilines Benzylamines Dialkylarylamines Phenylmethylamines Aralkylamines Aminopyridines and derivatives Pyridinones Secondary alkylarylamines Heteroaromatic compounds Lactams Ureas Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cytisine - 1-piperidinecarboxamide - Piperidinecarboxamide - Benzylamine - Phenylmethylamine - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Aminopyridine - Pyridinone - Secondary aliphatic/aromatic amine - Aralkylamine - Monocyclic benzene moiety - Pyridine - Piperidine - Benzenoid - Heteroaromatic compound - Tertiary amine - Urea - Lactam - Azacycle - Secondary amine - Organoheterocyclic compound - Amine - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - 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