Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC2=C1N[C@H]1[C@@H]3C[C@@H]4[C@H]5[C@H](C[C@]21[C@@H]5O)N3C\C4=C\C

InChIKey

InChIKey=HTETYMBEAKZXSG-JVCOJETQSA-N

Formula

C20H24N2O2

Mass

324.424

Export to:

JSON SDF CSV

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 - Dihydroindole - Indole or derivatives - Quinuclidine - Anisole - Aralkylamine - Secondary aliphatic/aromatic amine - Azepane - Alkyl aryl ether - Benzenoid - Piperidine - Cyclic alcohol - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Azacycle - Organoheterocyclic compound - Secondary amine - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - 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

Previous Back Next