Compound Identification
SMILES
C[C@@H](O)[C@]1(O)C[N+]23CC[C@]1(O)[C@]2(C)C1=C(CC3)C2=CC=CC=C2N1
InChIKey
InChIKey=BOSZMARBZFQIKI-SDONXPCWSA-N
Formula
C19H25N2O3
Mass
329.419
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
Beta carbolines 3-alkylindoles Aralkylamines Benzenoids N-alkylpyrrolidines Piperidines Heteroaromatic compounds Tertiary alcohols Tetraalkylammonium salts 1,3-aminoalcohols Pyrroles 1,2-diols Secondary alcohols 1,2-aminoalcohols Azacyclic compounds Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Stemmadenine-skeleton - Beta-carboline - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Aralkylamine - Piperidine - N-alkylpyrrolidine - Benzenoid - Tertiary alcohol - Heteroaromatic compound - Quaternary ammonium salt - Pyrrolidine - Pyrrole - 1,3-aminoalcohol - Tetraalkylammonium salt - 1,2-diol - Secondary alcohol - 1,2-aminoalcohol - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alcohol - 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