Structure Information
Structure

Compound Identification

SMILES

CN1CC[C@@H]2C[C@H](OC(=O)C3=CC(C(=O)O[C@H]4C[C@H]5CCN(C)[C@H]5[C@H]5[C@H]4OC(=O)C4=CC6=C(OCO6)C=C54)=C(C)N=C3C)[C@@H]3OC(=O)C4=CC5=C(OCO5)C=C4[C@H]3[C@H]12

InChIKey

InChIKey=CJYOGPFDNAEALZ-BVORSCEZSA-N

Formula

C43H43N3O12

Mass

793.826

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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 - Tetracarboxylic acid or derivatives - Benzopyran - Isochromane - 2-benzopyran - Benzodioxole - Indole or derivatives - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Methylpyridine - Aralkylamine - Pyridine - Benzenoid - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrolidine - Amino acid or derivatives - Carboxylic acid ester - Lactone - Tertiary amine - Tertiary aliphatic amine - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen 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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