Compound Identification
SMILES
COC1=CC2=C(C=C1)[C@]13C[C@H]4C([C@H]5C[C@@H]([C@@H]1N2C)N4C\C5=C\C)C3=O
InChIKey
InChIKey=LEHVAVBEMNLCAM-JHRDMWOESA-N
Formula
C21H24N2O2
Mass
336.435
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 Anisoles Azepanes Aralkylamines Alkyl aryl ethers Piperidines Trialkylamines Ketones Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Sarpagine-skeleton - Pyridoindole - Beta-carboline - Quinolizidine - Indole or derivatives - Anisole - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Quinuclidine - Phenol ether - Aralkylamine - Alkyl aryl ether - Azepane - Benzenoid - Piperidine - Tertiary aliphatic amine - Tertiary amine - Ketone - Azacycle - Ether - Organoheterocyclic compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Amine - Organooxygen compound - Organonitrogen compound - 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