Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C2C(=O)O[C@@H]3CC=C4CC[N+](C)([O-])[C@H]4[C@@H]3C2=C1

InChIKey

InChIKey=LAEQLQRWNDLBBU-KNFXUPHZSA-N

Formula

C18H21NO5

Mass

331.368

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Amaryllidaceae alkaloids

Subclass

Homolycorine-type amaryllidaceae alkaloids

Intermediate Tree Nodes

Not available

Direct Parent

Homolycorine-type amaryllidaceae alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Homolycorine skeleton - Benzopyran - Isochromane - 2-benzopyran - Indole or derivatives - Anisole - Phenol ether - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Trialkyl amine oxide - Pyrrolidine - Carboxylic acid ester - Lactone - Trisubstituted n-oxide - Organoheterocyclic compound - Azacycle - N-oxide - Oxacycle - Ether - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic salt - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as homolycorine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids.

External Descriptors

Not available

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