Compound Identification
SMILES
C[C@@H]1O[C@@H](O)C(C#COO)[C@H]2C[C@@H]3N(CC[C@@]33C(=O)NC4=CC=CC=C34)C[C@H]12
InChIKey
InChIKey=WMCSSTWQESHHGU-GBAZDDPASA-N
Formula
C21H24N2O5
Mass
384.432
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
Indolizidines Indolines Aralkylamines Piperidines Oxanes Benzenoids N-alkylpyrrolidines Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Organic hydroperoxides Lactams Hemiacetals Peroxols Oxacyclic compounds Azacyclic compounds Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Yohimban skeleton - Yohimbine alkaloid - Indole or derivatives - Dihydroindole - Indolizidine - Aralkylamine - Oxane - Piperidine - N-alkylpyrrolidine - Benzenoid - Pyrrolidine - Carboxamide group - Hemiacetal - Lactam - Hydroperoxide - Amino acid or derivatives - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Peroxol - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - 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