Structure Information
Structure

Compound Identification

SMILES

COC1=C(O)C=C2C3C4N(C)CCC4=CC(O)C3OC(=O)C2=C1

InChIKey

InChIKey=QOGSPMDZSUNSAJ-UHFFFAOYSA-N

Formula

C17H19NO5

Mass

317.341

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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 - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Tertiary amine - Secondary alcohol - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Ether - Oxacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - 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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