Structure Information
Structure

Compound Identification

SMILES

C\C=C1\CN2CC[C@]34[C@@H]2C[C@@H]1[C@@H]1C=C([C@H]2C[C@]56[C@@H]7C[C@@H](\C(CN27)=C/C)\C2=C\N7[C@H]8\C(=C/N([C@H]52)C2=CC=CC=C62)[C@H]2C[C@@H]5N(CC[C@@]85C5=CC=CC=C75)C\C2=C\C)C(=O)N([C@H]31)C1=CC=CC=C41

InChIKey

InChIKey=DXTTUINJHHYHFN-POYLYQTGSA-N

Formula

C59H60N6O

Mass

869.17

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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 - Stemmadenine-skeleton - Carbazole - Indolizidine - Indole or derivatives - Tertiary aliphatic/aromatic amine - Aralkylamine - Benzenoid - N-alkylpyrrolidine - Piperidine - Tertiary carboxylic acid amide - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Lactam - Carboxamide group - Amino acid or derivatives - Allylamine - Azacycle - Organoheterocyclic compound - Enamine - Carboxylic acid derivative - 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 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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