Structure Information
Structure

Compound Identification

SMILES

CCC1=C[N+]2=C(C=C1C1=CN3[C@H]4[C@H]([C@@H]1O)[C@H]1C[C@H]5[C@@]4(CC[N+]5(C)C\C1=C\CO)C1=CC=CC=C31)C1=C(CC2)C2=C(N1)C=CC=C2OC

InChIKey

InChIKey=MPBXTVZTOPAKIA-JFJSMFJZSA-O

Formula

C40H44N4O3

Mass

628.816

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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 - Beta-carboline - Carbazole - Pyridoindole - Quinolizine - 3-alkylindole - Indole - Indole or derivatives - Indolizidine - Tertiary aliphatic/aromatic amine - Anisole - Phenol ether - Tetrahydropyridine - Aralkylamine - Alkyl aryl ether - Benzenoid - N-alkylpyrrolidine - Piperidine - Pyridine - Pyridinium - Tetraalkylammonium salt - Heteroaromatic compound - Quaternary ammonium salt - Pyrrolidine - Pyrrole - Tertiary amine - Secondary alcohol - Ether - Enamine - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic cation - 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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