Compound Identification
SMILES
CC1OC(=O)CC2CC(=O)N(CCC3CN(C(=O)OCC4=CC=CC=C4)C4=CC=CC=C34)CC12
InChIKey
InChIKey=AMOLYMXAGMCJFB-UHFFFAOYSA-N
Formula
C27H30N2O5
Mass
462.546
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
Indolecarboxylic acids Benzyloxycarbonyls Piperidinones Delta lactams Delta valerolactones Oxanes Tertiary carboxylic acid amides Carbamate esters Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Oxacyclic compounds Organic oxides Carbonyl compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Yohimban skeleton - Yohimbine alkaloid - Indolecarboxylic acid - Indolecarboxylic acid derivative - Benzyloxycarbonyl - Indole or derivatives - Delta-lactam - Delta valerolactone - Delta_valerolactone - Piperidinone - Piperidine - Oxane - Benzenoid - Monocyclic benzene moiety - Carbamic acid ester - Tertiary carboxylic acid amide - Lactone - Lactam - Carboxamide group - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen 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