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Structure Information
Structure

Compound Identification

SMILES

CCCCC(O)(C(CC1=CC=CC=C1)C[N+]1(C)CC[N+](C)(C)CC1)C1=CC=CC=C1

InChIKey

InChIKey=ZREZKDCYDMXZFD-UHFFFAOYSA-N

Formula

C27H42N2O

Mass

410.645

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lignans, neolignans and related compounds

Class

Not available

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Lignans, neolignans and related compounds

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Norlignan skeleton - Linear 1,3-diarylpropanoid - Aralkylamine - N-alkylpiperazine - N-methylpiperazine - Monocyclic benzene moiety - 1,4-diazinane - Piperazine - Benzenoid - 1,3-aminoalcohol - Tetraalkylammonium salt - Quaternary ammonium salt - Tertiary alcohol - Azacycle - Organoheterocyclic compound - Alcohol - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Aromatic alcohol - Organic cation - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

External Descriptors

Not available

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