Compound Identification
SMILES
[K+].O[C@H]1C[C@H]2[C@@H](NC(=O)C3=CC4=C(OCO4)C=C23)[C@@H]2OP([O-])(=O)O[C@H]12
InChIKey
InChIKey=WRCBWSFOSWZXSS-PXRHWMLOSA-M
Formula
C14H13KNO8P
Mass
393.329
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Alternative Parents
Phenanthridines and derivatives Isoquinolones and derivatives Tetrahydroisoquinolines Benzodioxoles Benzenoids Organic phosphoric acids and derivatives Dioxaphospholanes Lactams Cyclic alcohols and derivatives Secondary alcohols Secondary carboxylic acid amides Oxacyclic compounds Acetals Azacyclic compounds Organic zwitterions Organic potassium salts Organopnictogen compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Isoquinolone - Quinoline - Tetrahydroisoquinoline - Benzodioxole - Organic phosphoric acid derivative - Benzenoid - Cyclic alcohol - 1,3_dioxaphospholane - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Organoheterocyclic compound - Acetal - Organic alkali metal salt - Azacycle - Carboxylic acid derivative - Oxacycle - Organic salt - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organic oxygen compound - Organic potassium salt - Organic zwitterion - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as phenanthridine- and phenanthridone-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds based on the phenanthridine or the phenanthridone skeleton. Phenanthridone-type alkaloids have the highest oxygenated C ring in all Amaryllidaceae alkaloids, and they always show an amide group in ring B. On the contrary, alkaloids of the phenanthridine type often show completely aromatic ring system, occasionally with a methylation quaternary nitrogen atom.
External Descriptors
Not available