Compound Identification
SMILES
COC1=C2O[C@H]3C[C@@H](OC(=O)C4=CC=C(C=C4)C(C)=O)C=C[C@]33CCN(C)CC(C=C1)=C23
InChIKey
InChIKey=GPVXFFHVVZVADA-YBXDKENTSA-N
Formula
C26H27NO5
Mass
433.504
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
Alkyl-phenylketones Benzazepines Benzoic acid esters Acetophenones Coumarans Benzoyl derivatives Aryl alkyl ketones Anisoles Azepines Aralkylamines Alkyl aryl ethers Carboxylic acid esters Amino acids and derivatives Trialkylamines Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Galanthamine-type amaryllidaceae alkaloid - Alkyl-phenylketone - Benzazepine - Benzoate ester - Acetophenone - Benzoic acid or derivatives - Phenylketone - Coumaran - Anisole - Benzoyl - Phenol ether - Aryl ketone - Aryl alkyl ketone - Aralkylamine - Alkyl aryl ether - Azepine - Benzenoid - Monocyclic benzene moiety - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Ketone - Carboxylic acid ester - Azacycle - Oxacycle - Ether - Carboxylic acid derivative - Organoheterocyclic compound - Amine - Organic oxygen compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen 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