Compound Identification
SMILES
Cl.CCCCCCCCOC(=O)C1=C[C@H](O)C[C@@H]2OC3=C(OC)C=CC4=C3[C@]12CCN(C)C4
InChIKey
InChIKey=DTHLJOSKECSBMR-CWJSREQFSA-N
Formula
C26H38ClNO5
Mass
480.04
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Galanthamine-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Galanthamine-type amaryllidaceae alkaloids
Alternative Parents
Benzazepines Coumarans Anisoles Alkyl aryl ethers Aralkylamines Azepines Enoate esters Trialkylamines Secondary alcohols Amino acids and derivatives Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Hydrochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Galanthamine-type amaryllidaceae alkaloid - Benzazepine - Coumaran - Anisole - Phenol ether - Alkyl aryl ether - Azepine - Aralkylamine - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Ether - Alcohol - Organonitrogen compound - Organooxygen compound - Carbonyl group - Hydrochloride - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as galanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A.
External Descriptors
Not available