Compound Identification
SMILES
C\C=C1/C[N+]2(C)[C@H]3CC4=C([N-]C5=CC=CC=C45)[C@@H]2C[C@H]1C3CO
InChIKey
InChIKey=RSVXMMBDAVLBGI-PANNUYMHSA-N
Formula
C20H24N2O
Mass
308.425
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Macroline alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Macroline alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Macroline alkaloids
Alternative Parents
Vobasan alkaloids Ajmaline-sarpagine alkaloids Beta carbolines 3-alkylindoles Quinuclidines Aralkylamines Piperidines Benzenoids Tetraalkylammonium salts Pyrroles 1,3-aminoalcohols Heteroaromatic compounds Azacyclic compounds Hydrocarbon derivatives Organic salts Organic zwitterions Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macroline skeleton - Sarpagine-skeleton - Vobasan skeleton - Beta-carboline - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Quinuclidine - Aralkylamine - Piperidine - Benzenoid - Tetraalkylammonium salt - Heteroaromatic compound - Pyrrole - Quaternary ammonium salt - 1,3-aminoalcohol - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic salt - Organic oxygen compound - Alcohol - Amine - Organic zwitterion - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.
External Descriptors
Not available