Structure Information
Structure

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

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Taxonomic Classification

Taxonomy Tree

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

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

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