Structure Information
Structure

Compound Identification

SMILES

[Br-].[Br-].OC\C=C1\C[N+]2(CC[C@H]3[C@@H]2C[C@@H]1C1=CN2[C@H]4[C@H]5[C@H]6C[C@H]7[C@@]4(CC[N+]7(CC6=CCO[C@H]5N([C@H]31)c1ccccc1)C1CCCC=C1)c1ccccc21)C1CCCC=C1

InChIKey

InChIKey=HIKALAMHAXPLDW-MZUDCFAUSA-L

Formula

C50H60Br2N4O2

Mass

908.864

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Strychnos alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Strychnos alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Strychnan skeleton - Akuammicine-skeleton - Curan skeleton - Stemmadenine-skeleton - Carbazole - Indole or derivatives - Indolizidine - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Aralkylamine - Monocyclic benzene moiety - Piperidine - Benzenoid - N-alkylpyrrolidine - Tetraalkylammonium salt - Pyrrolidine - Quaternary ammonium salt - Tertiary amine - Oxacycle - Enamine - Allylamine - Azacycle - Organoheterocyclic compound - Alcohol - Primary alcohol - Organic salt - Organooxygen compound - Organonitrogen compound - Organic zwitterion - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Amine - Organic bromide salt - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

External Descriptors

Not available

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