Compound Identification
SMILES
CC[C@H]1[C@@H]2C[C@@H]3N([C@@H]4C2C(O)O[C@@H]4C2=C3N(C)C3=CC=CC=C23)[C@@H]1O
InChIKey
InChIKey=LCYYYYGFLZJERP-LHNICRNFSA-N
Formula
C20H24N2O3
Mass
340.423
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 N-alkylindoles Quinuclidines Piperidines N-methylpyrroles Benzenoids Oxolanes Heteroaromatic compounds Hemiacetals Hemiaminals Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macroline skeleton - Sarpagine-skeleton - Vobasan skeleton - Beta-carboline - Pyridoindole - N-alkylindole - 3-alkylindole - Indole - Indole or derivatives - Quinuclidine - N-methylpyrrole - Piperidine - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Oxolane - Pyrrole - Hemiaminal - Hemiacetal - Alkanolamine - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - 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