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
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 Indolines Quinuclidines Azepanes Piperidines Tertiary alcohols Pyrrolidines Amino acids and derivatives Carboxylic acid esters Alkanolamines Polyols Azacyclic compounds Dialkylamines Monocarboxylic acids and derivatives Organic oxides Organopnictogen compounds Hydrocarbon derivatives Carbonyl compounds
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