Compound Identification
SMILES
CN(C)C1=CC=C(C=C1)C1=C2[C@@H]3C[C@H](CN2C(=O)C=C1)C[NH+](C3)C1CCOCC1
InChIKey
InChIKey=GDDXEQDRXQRWDM-PKOBYXMFSA-O
Formula
C24H32N3O2
Mass
394.538
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
Phenylpyridines Aniline and substituted anilines Dialkylarylamines Aralkylamines Pyridinones Piperidines Oxanes Heteroaromatic compounds Quaternary ammonium salts Trialkylamines Lactams Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cytisine - 3-phenylpyridine - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Pyridinone - Aralkylamine - Oxane - Piperidine - Pyridine - Benzenoid - Monocyclic benzene moiety - Quaternary ammonium salt - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Lactam - Dialkyl ether - Azacycle - Oxacycle - Organoheterocyclic compound - Ether - Amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organic cation - 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