Structure Information
Structure

Compound Identification

SMILES

[OH-].CCC1=C[N+]2=C(C=C1C1=CN3[C@H]4[C@H]([C@@H]1O)[C@H]1C[C@@H]5N(CC[C@]45C4=CC=CC=C34)C\C1=C\CO)C1=C(CC2)C2=CC=CC=C2N1

InChIKey

InChIKey=LNYYVGPSHGDMOY-WKAYOMBLSA-N

Formula

C38H40N4O3

Mass

600.763

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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 - Beta-carboline - Carbazole - Pyridoindole - Quinolizine - 3-alkylindole - Indole - Indole or derivatives - Indolizidine - Tertiary aliphatic/aromatic amine - Tetrahydropyridine - Aralkylamine - N-alkylpyrrolidine - Pyridinium - Piperidine - Pyridine - Benzenoid - Pyrrole - Heteroaromatic compound - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Enamine - Azacycle - Organoheterocyclic compound - Alcohol - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic hydroxide - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - 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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