Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CC(NC(=O)C2=CC(NC(=O)C3=CC(F)=CC=C3)C(O)C(O)C2)C(N)=O)C=C1

InChIKey

InChIKey=MNNLOBMQPWEGDP-UHFFFAOYSA-N

Formula

C24H26FN3O6

Mass

471.485

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Amaryllidaceae alkaloids

Subclass

Norbelladine-type amaryllidaceae alkaloids

Intermediate Tree Nodes

Not available

Direct Parent

Norbelladine-type amaryllidaceae alkaloids

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Norbelladine skeleton - Phenylalanine or derivatives - N-acyl-alpha amino acid or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzoic acid or derivatives - Benzamide - Methoxybenzene - Benzoyl - Phenoxy compound - Anisole - Phenol ether - Fluorobenzene - Halobenzene - Alkyl aryl ether - Aryl fluoride - Aryl halide - Fatty acyl - Fatty amide - Monocyclic benzene moiety - Benzenoid - Secondary carboxylic acid amide - 1,2-diol - Carboxamide group - Secondary alcohol - Primary carboxylic acid amide - Ether - Carboxylic acid derivative - Organopnictogen compound - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Carbonyl group - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as norbelladine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the norbelladine skeleton. They are derived initially from the condensation of tyramine and protocatechuic aldehyde or its derivatives in plants.

External Descriptors

Not available

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