Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCC[N+]12[C@H]3C[C@]45[C@@H](O)C3[C@H](CC1[C@@H]4N(C)c1ccccc51)[C@H](CC)[C@H]2O

InChIKey

InChIKey=HULQLTYDKCDRDQ-GGHMJNQHSA-N

Formula

C29H45N2O2

Mass

453.69

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Ajmaline-sarpagine alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Ajmaline-sarpagine alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Sarpagine-skeleton - Pyridoindole - Beta-carboline - Quinolizidine - Indole or derivatives - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Quinuclidine - Aralkylamine - Azepane - Benzenoid - Piperidine - Tetraalkylammonium salt - Cyclic alcohol - Tertiary amine - Secondary alcohol - Hemiaminal - Azacycle - Organoheterocyclic compound - Alkanolamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as ajmaline-sarpagine alkaloids. These are organic compounds containing either of the ajmalan, sarpagan skeleton, or derivative thereof. The Sarpagine (Akuammidine) group, based on the sarpagan nucleus, arises from bond formation between C-16 and C-5 of the corynantheine precursor. Ajmaline alkaloids are based on a 17,19-secoyohimban skeleton (oxayohimban) which is invariably present as an ether.

External Descriptors

Not available

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