Compound Identification
SMILES
CC[C@@H]1CN2CC[C@]34[C@@H](CO)[C@H]1CC2C3=NC1=CC=CC=C41
InChIKey
InChIKey=PYMHIOSGBXFQPS-HXRBAIRESA-N
Formula
C19H24N2O
Mass
296.414
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 Aralkylamines Piperidines Benzenoids Trialkylamines Ketimines Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Akuammilan skeleton - Quinolizidine - 3-alkylindole - Indole or derivatives - Aralkylamine - Piperidine - Benzenoid - Ketimine - Tertiary amine - Tertiary aliphatic amine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Amine - Alcohol - Primary alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Imine - 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