Compound Identification
SMILES
COC(=O)C1C2CC3C4NC5=CC=CC=C5C4CCN3CC2C(C)OC1C1C2C(CN3C=CC4=C5C=CC=CC5=NC4=C13)C(C)OC=C2C(=O)OC
InChIKey
InChIKey=DZCKWORLHZZPNE-UHFFFAOYSA-N
Formula
C42H46N4O6
Mass
702.852
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 Quinolizidines Indoles Indolines Secondary alkylarylamines Aralkylamines Pyridines and derivatives Piperidines Oxanes Benzenoids Dicarboxylic acids and derivatives Vinylogous esters Methyl esters Enoate esters Heteroaromatic compounds Pyrroles Trialkylamines Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Dialkyl ethers Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Ajmalicine-skeleton - 18-oxayohimban - Corynanthean skeleton - Yohimban skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - Quinolizidine - Indole - Indole or derivatives - Dihydroindole - Secondary aliphatic/aromatic amine - Aralkylamine - Benzenoid - Dicarboxylic acid or derivatives - Oxane - Piperidine - Pyridine - Methyl ester - Vinylogous ester - Heteroaromatic compound - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Pyrrole - Carboxylic acid ester - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Dialkyl ether - Carboxylic acid derivative - Ether - Organoheterocyclic compound - Secondary amine - Azacycle - Oxacycle - Amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organic nitrogen 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