Structure Information
Structure

Compound Identification

SMILES

COC1=CC(OC)=C(CN(CCC2=CC(OC)=C(OC)C=C2)CC2=NC(=CS2)C(=O)N2CC(C)OC(C)C2)C=C1

InChIKey

InChIKey=PQFNANUWHPIXAJ-UHFFFAOYSA-N

Formula

C30H39N3O6S

Mass

569.72

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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 heteromonocyclic compounds

Substituents

Norbelladine skeleton - Dimethoxybenzene - O-dimethoxybenzene - M-dimethoxybenzene - Phenethylamine - Morpholine-4-carboxylic acid or derivatives - 2-heteroaryl carboxamide - Phenol ether - Thiazolecarboxylic acid or derivatives - Benzylamine - Phenylmethylamine - Thiazolecarboxamide - Anisole - Methoxybenzene - Phenoxy compound - Alkyl aryl ether - 2,4-disubstituted 1,3-thiazole - Aralkylamine - Benzenoid - Oxazinane - Morpholine - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Thiazole - Tertiary carboxylic acid amide - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Amine - Organonitrogen compound - Organic oxide - Aromatic heteromonocyclic 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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