CC[C@H]1C2C[C@H]3[C@@H]4N(C)C5=CC=CC=C5C44C[C@@H](C2[C@H]4O)[N+]3([O-])[C@@H]1O

InChIKey=PTVVENUAISCPLQ-SPHUJYHJSA-N

C20H26N2O3

342.439

Organic compounds

Alkaloids and derivatives

Ajmaline-sarpagine alkaloids

Not available

Not available

Ajmaline-sarpagine alkaloids

Beta carbolines Quinolizidines Quinuclidines Dialkylarylamines Aralkylamines Azepanes Piperidines Benzenoids Trialkyl amine oxides Secondary alcohols Hemiaminals Cyclic alcohols and derivatives Trisubstituted amine oxides and derivatives Azacyclic compounds Organopnictogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Sarpagine-skeleton - Beta-carboline - Pyridoindole - Quinolizidine - Indole or derivatives - Quinuclidine - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Azepane - Aralkylamine - Benzenoid - Piperidine - Trialkyl amine oxide - Cyclic alcohol - Tertiary amine - Secondary alcohol - Hemiaminal - Organoheterocyclic compound - Trisubstituted n-oxide - Azacycle - Alkanolamine - N-oxide - Alcohol - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Aromatic heteropolycyclic compound

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.

Not available