CC[C@H]1C2C[C@H]3[C@@H]4N(C)C5=CC=CC=C5C44C[C@@H](C2[C@H]4O)[N@@+]3(CC2=CC=CC=C2)[C@@H]1O

InChIKey=KIPHTHYSVQAMJV-UHMKQIRJSA-N

C27H33N2O2

417.572

Organic compounds

Alkaloids and derivatives

Ajmaline-sarpagine alkaloids

Not available

Not available

Ajmaline-sarpagine alkaloids

N-benzylpiperidines Beta carbolines Quinolizidines Quinuclidines Dialkylarylamines Aralkylamines Azepanes Benzene and substituted derivatives Tetraalkylammonium salts Secondary alcohols Hemiaminals Cyclic alcohols and derivatives Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Organic salts Organic cations

Aromatic heteropolycyclic compounds

Sarpagine-skeleton - Beta-carboline - N-benzylpiperidine - Pyridoindole - Benzylpiperidine - Quinolizidine - Indole or derivatives - Dialkylarylamine - Quinuclidine - Tertiary aliphatic/aromatic amine - Azepane - Aralkylamine - Monocyclic benzene moiety - Piperidine - Benzenoid - Tetraalkylammonium salt - Cyclic alcohol - Secondary alcohol - Tertiary amine - Hemiaminal - Organoheterocyclic compound - Alkanolamine - Azacycle - Organic salt - Organooxygen compound - Hydrocarbon derivative - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Amine - Organic cation - 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