Structure Information
Structure

Compound Identification

SMILES

[H]C(C)(O)CC(=O)OC1([H])CC2([H])CCN(C)C2([H])C2([H])C3=CC4=C(OCO4)C=C3C(=O)OC12[H]

InChIKey

InChIKey=QYVZOJWDWWFSQK-UHFFFAOYSA-N

Formula

C21H25NO7

Mass

403.431

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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 - Benzodioxole - Beta-hydroxy acid - Fatty acid ester - Aralkylamine - Dicarboxylic acid or derivatives - N-alkylpyrrolidine - Benzenoid - Hydroxy acid - Fatty acyl - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Lactone - Carboxylic acid ester - Amino acid or derivatives - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Acetal - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Alcohol - 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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