Compound Identification
SMILES
CN(C)C1=CC=C(C=C1)C1=C2[C@@H]3C[C@@H](CN(C3)C(=O)C3=CC=NC=C3)CN2C(=O)C=C1
InChIKey
InChIKey=CFAXDEOSTPMWEV-FXAWDEMLSA-N
Formula
C25H26N4O2
Mass
414.509
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 Pyridinecarboxylic acids and derivatives N-acylpiperidines Dialkylarylamines Aniline and substituted anilines Pyridinones Tertiary carboxylic acid amides Heteroaromatic compounds Lactams Amino acids and derivatives Azacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cytisine - 3-phenylpyridine - N-acyl-piperidine - Pyridine carboxylic acid or derivatives - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Pyridinone - Monocyclic benzene moiety - Piperidine - Pyridine - Benzenoid - Tertiary carboxylic acid amide - Heteroaromatic compound - Tertiary amine - Carboxamide group - Lactam - Amino acid or derivatives - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - 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