Structure Information
Structure

Compound Identification

SMILES

[Zn++].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.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=SFIGEEQTMAWFAU-SWLXQBBLSA-L

Formula

C28H22N2O18P2Zn

Mass

801.81

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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

Not available

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 - Organic transition metal salt - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Acetal - Organic salt - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organopnictogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organic zwitterion - Organic oxide - 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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