Compound Identification
SMILES
CC=C1C(O)N2C3CC45C(NC6=C4C(O)C(O)C=C6)C2CC1C3C5OC(C)=O
InChIKey
InChIKey=DXFWECOXZKWCHA-UHFFFAOYSA-N
Formula
C21H26N2O5
Mass
386.448
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
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
Quinolizidines Indoles and derivatives Quinuclidines Azepanes Piperidines Pyrrolines Secondary alcohols 1,2-diols Amino acids and derivatives Carboxylic acid esters Alkanolamines Monocarboxylic acids and derivatives Enamines Dialkylamines Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Sarpagine-skeleton - Quinolizidine - Indole or derivatives - Quinuclidine - Azepane - Piperidine - Pyrroline - 1,2-diol - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Secondary amine - Polyol - Organoheterocyclic compound - Azacycle - Alkanolamine - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Enamine - Secondary aliphatic amine - Hydrocarbon derivative - Alcohol - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Amine - Organonitrogen compound - Organooxygen compound - Organic oxide - 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