Compound Identification
SMILES
[Mg++].O[C@H]1C=C2[C@@H](NC(=O)C3=C(O)C4=C(OCO4)C=C23)[C@@H]2OP([O-])(=O)O[C@H]12
InChIKey
InChIKey=UDKXXVPLESNRQD-WAJBGZTRSA-M
Formula
C14H11MgNO9P
Mass
392.518
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 1-hydroxy-4-unsubstituted benzenoids Organic phosphoric acids and derivatives Vinylogous acids Dioxaphospholanes Lactams Secondary alcohols Secondary carboxylic acid amides Azacyclic compounds Acetals Oxacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Isoquinolone - Quinoline - Tetrahydroisoquinoline - Benzodioxole - 1-hydroxy-4-unsubstituted benzenoid - Organic phosphoric acid derivative - Benzenoid - 1,3_dioxaphospholane - Vinylogous acid - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Azacycle - Oxacycle - Carboxylic acid derivative - Acetal - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organic salt - Organic cation - 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