Compound Identification
SMILES
CO[C@H]1C[C@]23[C@@H]([C@H]4C[C@H](N1C\C4=C\C)C2=NC1=C3C=C(OC)C=C1)C(=O)OC
InChIKey
InChIKey=GYXKWMZZGGJDCD-QMUBFCDFSA-N
Formula
C22H26N2O4
Mass
382.46
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Akuammilan and related alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Akuammilan and related alkaloids
Alternative Parents
Quinolizidines 3-alkylindoles Anisoles Alkyl aryl ethers Piperidines Methyl esters Ketimines Hemiaminals Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Akuammilan skeleton - 3-alkylindole - Quinolizidine - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Benzenoid - Piperidine - Methyl ester - Carboxylic acid ester - Hemiaminal - Ketimine - Carboxylic acid derivative - Ether - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Organic oxygen compound - Imine - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as akuammilan and related alkaloids. These are alkaloids with a structure based on either the akuammilan skeleton. The ring system in this group is formed from a precursor of the corynantheine type by bond formation between C-16 and C-7. Variations in this subgroup include, among others, alkaloids derived by C-3 to N-4 bond fission, as well as alkaloids in which the N-4 to C-5 bond in the Akuammiline skeleton has been severed.
External Descriptors
Not available