Compound Identification
SMILES
C1CNCCN1.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=AZMYEUOKLQUVDG-WAJBGZTRSA-N
Formula
C18H22N3O9P
Mass
455.36
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 Piperazines Vinylogous acids Dioxaphospholanes Lactams Secondary alcohols Secondary carboxylic acid amides Polyols Acetals Dialkylamines Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Organopnictogen compounds
Molecular Framework
Not available
Substituents
Phenanthridone-type amaryllidaceae alkaloid - Benzoquinoline - Phenanthridine - Isoquinolone - Quinoline - Tetrahydroisoquinoline - Benzodioxole - 1-hydroxy-4-unsubstituted benzenoid - 1,4-diazinane - Organic phosphoric acid derivative - Piperazine - Benzenoid - Vinylogous acid - 1,3_dioxaphospholane - Carboxamide group - Secondary carboxylic acid amide - Lactam - Secondary alcohol - Secondary amine - Polyol - Azacycle - Carboxylic acid derivative - Secondary aliphatic amine - Oxacycle - Acetal - Organoheterocyclic compound - Amine - Organopnictogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - 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