Compound Identification
SMILES
COC(=O)N1C2=C(C=CC(OC)=C2)C2CCN3C[C@@H]4CCCC[C@H]4C[C@@]3(OC(=O)C3=CC(OC)=C(OC)C(OC)=C3)[C@@]12OC
InChIKey
InChIKey=NVIWXHZVAUUACU-SPCQBKQQSA-N
Formula
C33H42N2O9
Mass
610.704
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 Indolecarboxylic acids Gallic acid and derivatives P-methoxybenzoic acids and derivatives M-methoxybenzoic acids and derivatives Quinolizidines Benzoic acid esters Phenoxy compounds Anisoles Methoxybenzenes Benzoyl derivatives Alkyl aryl ethers Piperidines Carbamate esters Carboxylic acid esters Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Yohimban skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - Gallic acid or derivatives - Indolecarboxylic acid - Indolecarboxylic acid derivative - M-methoxybenzoic acid or derivatives - P-methoxybenzoic acid or derivatives - Benzoate ester - Quinolizidine - Benzoic acid or derivatives - Indole or derivatives - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - Benzoyl - Alkyl aryl ether - Piperidine - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organic oxide - 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