Compound Identification
SMILES
[Br-].[Br-].C(C1CO1)[N+]12CC[C@@]34[C@@H]1C[C@@H]1[C@@H]5[C@@H]3N([C@@H]3OCC=C6C[N+]7(CC8CO8)CC[C@@]89[C@@H]7C[C@@H]6[C@@H]3[C@@H]8N([C@@H]5OCC=C1C2)C1=CC=CC=C91)C1=CC=CC=C41
InChIKey
InChIKey=LESLJOIPWJJEBA-KFPQGFPQSA-L
Formula
C44H50Br2N4O4
Mass
858.716
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
Curan alkaloids Carbazoles Indolizidines Dialkylarylamines Aralkylamines Piperidines N-alkylpyrrolidines Benzenoids Tetraalkylammonium salts Oxacyclic compounds Azacyclic compounds Epoxides Dialkyl ethers Organic bromide salts Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Strychnan skeleton - Akuammicine-skeleton - Curan skeleton - Stemmadenine-skeleton - Carbazole - Indole or derivatives - Indolizidine - Dialkylarylamine - Aralkylamine - Piperidine - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Quaternary ammonium salt - Tetraalkylammonium salt - Azacycle - Dialkyl ether - Oxirane - Ether - Organoheterocyclic compound - Oxacycle - Organonitrogen compound - Amine - Organic oxygen compound - Organooxygen compound - Organic bromide salt - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Organic cation - 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