Structure Information
Structure

Compound Identification

SMILES

COC1=CC(=CC(OC)=C1O)[C@@H]1[C@H]2[C@@H](COC2=O)[C@@H](NC2CC(C)(C)N([O])C(C)(C)C2)C2=CC3=C(OCO3)C=C12

InChIKey

InChIKey=MNYFRPDQBQTHSV-IWRQBJDLSA-N

Formula

C30H37N2O8

Mass

553.632

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lignans, neolignans and related compounds

Class

Lignan lactones

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Lignan lactones

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Lignan lactone - 1-aryltetralin lignan - Tametraline - Linear furanonaphthodioxole - Naphthofuran - M-dimethoxybenzene - Dimethoxybenzene - Tetralin - Methoxyphenol - Benzodioxole - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - Aralkylamine - Phenol - 4-aminopiperidine - Alkyl aryl ether - Benzenoid - Piperidine - Gamma butyrolactone - Monocyclic benzene moiety - Tetrahydrofuran - Lactone - Carboxylic acid ester - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Monocarboxylic acid or derivatives - Ether - Secondary aliphatic amine - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as lignan lactones. These are lignans that contain a lactone moiety. They include 1-aryltetralin lactones, dibenzylbutyrolactone lignans, and podophyllotoxins, among others.

External Descriptors

Not available

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