Compound Identification
SMILES
[Cl-].COC(=O)C1C(O)CCC2C[NH+]3CCC4=C(NC5=CC=CC=C45)C3CC12
InChIKey
InChIKey=PIPZGJSEDRMUAW-UHFFFAOYSA-N
Formula
C21H27ClN2O3
Mass
390.91
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
Corynanthean-type alkaloids Beta carbolines Delta amino acids and derivatives 3-alkylindoles Aralkylamines Beta hydroxy acids and derivatives Piperidines Benzenoids Pyrroles Methyl esters Heteroaromatic compounds Trialkylamines Secondary alcohols Cyclic alcohols and derivatives Azacyclic compounds Monocarboxylic acids and derivatives Carbonyl compounds Hydrocarbon derivatives Organic chloride salts Organic oxides Organic zwitterions Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Yohimbine - Corynanthean skeleton - Yohimbine alkaloid - Beta-carboline - Delta amino acid or derivatives - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Beta-hydroxy acid - Aralkylamine - Hydroxy acid - Piperidine - Benzenoid - Cyclic alcohol - Heteroaromatic compound - Pyrrole - Methyl ester - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Tertiary aliphatic amine - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic zwitterion - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organic chloride salt - Organic salt - 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