Compound Identification
SMILES
Cl.CCC1C2CC3C4N(C)C5=CC=CC=C5C44CC(C2C4O)N3C1O
InChIKey
InChIKey=FNCWZVOLGCRECX-UHFFFAOYSA-N
Formula
C20H27ClN2O2
Mass
362.9
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
Beta carbolines Quinolizidines Quinuclidines Dialkylarylamines Azepanes Aralkylamines Piperidines Benzenoids Secondary alcohols Hemiaminals Cyclic alcohols and derivatives Azacyclic compounds Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Sarpagine-skeleton - Beta-carboline - Pyridoindole - Quinolizidine - Indole or derivatives - Quinuclidine - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Azepane - Aralkylamine - Benzenoid - Piperidine - Cyclic alcohol - Tertiary amine - Secondary alcohol - Hemiaminal - Organoheterocyclic compound - Azacycle - Alkanolamine - Alcohol - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Hydrochloride - 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