Compound Identification
SMILES
COC1=C2O[C@H]3C[C@@H](OP(=O)(SCCO)N(CCCl)CCCl)C=C[C@]33CCN(C)CC(C=C1)=C23
InChIKey
InChIKey=PKDPVQWADNMFLC-KQYVQNMBSA-N
Formula
C23H33Cl2N2O5PS
Mass
551.46
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 Nitrogen mustard compounds Alkyl aryl ethers Aralkylamines Azepines Trialkylamines Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Organothiophosphorus compounds Primary alcohols Alkyl chlorides Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Galanthamine-type amaryllidaceae alkaloid - Benzazepine - Coumaran - Anisole - Nitrogen mustard - Phenol ether - Alkyl aryl ether - Azepine - Aralkylamine - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Sulfenyl compound - Azacycle - Oxacycle - Organothiophosphorus compound - Ether - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxide - Organosulfur compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Amine - Alkyl halide - Alkyl chloride - Hydrocarbon derivative - 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