Structure Information
Structure

Compound Identification

SMILES

CCC1C2CC3C4N(C(C)=O)C5=CC=CC=C5[C@]44CC([C@@H]2[C@H]4OC(C)=O)N3[C@@H]1OC(C)=O

InChIKey

InChIKey=KRFLHCYRCOUVOX-DTIBIAKCSA-N

Formula

C25H30N2O5

Mass

438.524

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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 - Quinuclidine - Azepane - Benzenoid - Piperidine - Dicarboxylic acid or derivatives - Acetamide - Tertiary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - 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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