Structure Information
Structure

Compound Identification

SMILES

CC[C@@]12C[C@H]3CN4C5=CC=CC=C5C56CCN7C[C@H]8O[C@H]8[C@@](CC)(C[C@H]8CN9C%10=CC=CC=C%10C%10(CCN(C[C@H]%11O[C@@H]1%11)[C@@H]2%10)C39OC458)[C@@H]67

InChIKey

InChIKey=UMIVYNNQXZYFTJ-PFYVAAJMSA-N

Formula

C40H46N4O3

Mass

630.833

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Aspidospermatan-type alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Aspidospermatan-type alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Aspidosperma alkaloid - Plumeran-type alkaloid - Carbazole - Quinolidine - Indolizidine - Indole or derivatives - Dialkylarylamine - Aralkylamine - Epoxypiperidine - Para-oxazepine - Benzenoid - N-alkylpyrrolidine - Piperidine - Oxazinane - 1,3-oxazinane - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as aspidospermatan-type alkaloids. These are tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids.

External Descriptors

Not available

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