Compound Identification
SMILES
C\C=C1/CN2CC[C@]34[C@@H]2C[C@@H]1[C@H](C=O)[C@@H]3N(C(C)=O)C1=CC=CC=C41
InChIKey
InChIKey=VVJAXIGCVFZTKR-XMSVKNKBSA-N
Formula
C21H24N2O2
Mass
336.435
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Strychnos alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Strychnos alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Strychnos alkaloids
Alternative Parents
Carbazoles Indolizidines Aralkylamines Piperidines N-alkylpyrrolidines Benzenoids Tertiary carboxylic acid amides Acetamides Trialkylamines Amino acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Strychnan skeleton - Akuammicine-skeleton - Stemmadenine-skeleton - Carbazole - Indolizidine - Indole or derivatives - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Piperidine - Acetamide - Tertiary carboxylic acid amide - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Aldehyde - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.
External Descriptors
Not available