Structure Information
Structure

Compound Identification

SMILES

COC1C(OC(C)=O)C2CCN3CC4=CC(OC)=C(OC)C=C4C(C23)C1OC(C)=O

InChIKey

InChIKey=MBTDPNXHRNXILX-UHFFFAOYSA-N

Formula

C22H29NO7

Mass

419.474

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Amaryllidaceae alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Amaryllidaceae alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Amaryllidaceae alkaloid - Galanthan skeleton - Benzoquinoline - Phenanthridine - Quinoline - Tetrahydroisoquinoline - Indole or derivatives - Anisole - Alkyl aryl ether - Aralkylamine - Dicarboxylic acid or derivatives - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as amaryllidaceae alkaloids. These are isoquinoline alkaloids with a skeleton deriving from lycorine, norbelladine, homolycorine, hemanthamine, crinine, tazettine, montanine, plicamine, galanthindole, galanthamine, gracilline, among others. Amaryllidaceae Alkaloids represent a large group of biogenetically related isoquinoline alkaloids that are found exclusively in plants belonging to this family of Amaryllidaceae. This group of alkaloids is also derived from two tyrosine units which combine, with loss of one carbon atom, to give a benzylphenylethylamine precursor unit, e.g. Norbelladine, which by various oxidative cyclisation processes, prominent among which are phenol oxidative coupling reactions, can give rise to the nine major skeletal groups.

External Descriptors

Not available

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