Compound Identification
SMILES
COC1=CC2=C(N([C@H]3C[C@H]4CCN5CC[C@@]23[C@]52OCC=C42)C(C)=O)C(O)=C1
InChIKey
InChIKey=XORSOONLULVOCT-WTXAKBKRSA-N
Formula
C21H24N2O4
Mass
368.433
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 Anisoles 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Piperidines N-alkylpyrrolidines Tertiary carboxylic acid amides Dihydrofurans Acetamides Oxacyclic compounds Azacyclic compounds Amines Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Stemmadenine-skeleton - Carbazole - Indole or derivatives - Indolizidine - Anisole - Phenol ether - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Piperidine - Benzenoid - N-alkylpyrrolidine - Dihydrofuran - Acetamide - Pyrrolidine - Tertiary carboxylic acid amide - Carboxamide group - Azacycle - Oxacycle - Ether - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Amine - Organic oxygen compound - 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