Compound Identification
SMILES
C\C=C1\CN2[C@H]3CC4=C(NC5=C4C=C(O)C=C5)[C@@H]2C[C@H]1C3CO
InChIKey
InChIKey=VTVQHYQGTTVKDE-VWFUFAFFSA-N
Formula
C19H22N2O2
Mass
310.397
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 Hydroxyindoles Quinuclidines 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Piperidines 1,3-aminoalcohols Pyrroles Heteroaromatic compounds Trialkylamines Azacyclic compounds Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macroline skeleton - Sarpagine-skeleton - Vobasan skeleton - Beta-carboline - Pyridoindole - Hydroxyindole - 3-alkylindole - Indole - Indole or derivatives - Quinuclidine - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Benzenoid - Piperidine - 1,3-aminoalcohol - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Primary alcohol - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Amine - Organic nitrogen compound - Alcohol - 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