Compound Identification
SMILES
COC(=O)C1C(O)O[C@H](C)C2=CN3CCC4=C(NC5=CC=CC=C45)[C@@H]3C[C@H]12
InChIKey
InChIKey=VNZAGMCDYZBYNC-YCPBRXDTSA-N
Formula
C21H24N2O4
Mass
368.433
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 3-alkylindoles Tetrahydropyridines Beta hydroxy acids and derivatives Aralkylamines Oxanes Benzenoids Pyrroles Methyl esters Heteroaromatic compounds Trialkylamines Hemiacetals Amino acids and derivatives Oxacyclic compounds Monocarboxylic acids and derivatives Enamines Azacyclic compounds Allylamines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
18-oxayohimban - Ajmalicine-skeleton - Corynanthean skeleton - Yohimbine alkaloid - Pyridoindole - Beta-carboline - 3-alkylindole - Indole or derivatives - Indole - Aralkylamine - Tetrahydropyridine - Beta-hydroxy acid - Benzenoid - Oxane - Hydroxy acid - Heteroaromatic compound - Methyl ester - Pyrrole - Tertiary aliphatic amine - Tertiary amine - Hemiacetal - Carboxylic acid ester - Amino acid or derivatives - Allylamine - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Enamine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - 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