Compound Identification
SMILES
COC1=C2O[C@H]3C[C@@H](OC(=O)C45CCC(C)(C(=O)O4)C5(C)C)C=C[C@]33CCN(C)CC(C=C1)=C23
InChIKey
InChIKey=NEOVZHCREOELKA-UQTLHVISSA-N
Formula
C27H33NO6
Mass
467.562
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 Delta valerolactones Gamma butyrolactones Dicarboxylic acids and derivatives Pyrans Oxanes Oxolanes Amino acids and derivatives Carboxylic acid esters Trialkylamines Azacyclic compounds Oxacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Galanthamine-type amaryllidaceae alkaloid - Benzazepine - Coumaran - Anisole - Phenol ether - Alkyl aryl ether - Delta_valerolactone - Azepine - Aralkylamine - Delta valerolactone - Gamma butyrolactone - Dicarboxylic acid or derivatives - Oxane - Pyran - Benzenoid - Oxolane - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Ether - Amine - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organooxygen compound - Organonitrogen 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