Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1O[C@@H]2CC=C3CC[N+](C)([O-])[C@H]3[C@@H]2C2=CC(OC)=C(OC)C=C12

InChIKey

InChIKey=MYBKBZCVRIHHSP-VTFUZUOQSA-N

Formula

C19H25NO5

Mass

347.411

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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 - Alkyl aryl ether - N-alkylpyrrolidine - Benzenoid - Trialkyl amine oxide - Pyrrolidine - Acetal - N-oxide - Ether - Oxacycle - Trisubstituted n-oxide - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - 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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