Compound Identification
SMILES
O=C1CC[C@@H]2CN3CC[C@H]4[C@H](NC5=CC=CC=C45)[C@H]3C[C@H]2C1
InChIKey
InChIKey=NKWCIOQECZLITF-CGZJWMQNSA-N
Formula
C19H24N2O
Mass
296.414
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Yohimbine alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Yohimbine alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Yohimbine alkaloids
Alternative Parents
Beta carbolines Isoquinolones and derivatives Quinolizidines Indolines Secondary alkylarylamines Aralkylamines Piperidines Benzenoids Trialkylamines Cyclic ketones Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Yohimbine alkaloid - Yohimban skeleton - Beta-carboline - Pyridoindole - Isoquinolone - Quinolizidine - Indole or derivatives - Dihydroindole - Aralkylamine - Secondary aliphatic/aromatic amine - Piperidine - Benzenoid - Ketone - Cyclic ketone - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Secondary amine - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.
External Descriptors
Not available