Structure Information
Structure

Compound Identification

SMILES

CC=C1C(O)N2C3CC45C(NC6(O)C=CC=CC46O)C2CC1C3C5OC(C)=O

InChIKey

InChIKey=DIYCQDUCCGZWHL-UHFFFAOYSA-N

Formula

C21H26N2O5

Mass

386.448

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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

Aliphatic heteropolycyclic compounds

Substituents

Sarpagine-skeleton - Quinolizidine - Indole or derivatives - Dihydroindole - Quinuclidine - Azepane - Piperidine - Pyrrolidine - Tertiary alcohol - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Polyol - Carboxylic acid derivative - Alkanolamine - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - Alcohol - Aliphatic 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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