rhazinicine and 3-ethylpyridine

Four alkaloids comprising two vallesamine, one strychnan, and one pyranopyridine alkaloid, in addition to 32 other known alkaloids were isolated from two Malayan Alstonia species, Alstonia pneumatophora and Alstonia rostrata. The structures of these alkaloids were determined using NMR and MS analyses, and in one instance, confirmed by X-ray diffraction analysis. The nor-6,7-secovallesamine alkaloid, pneumatophorine, is notable for an unusual incorporation of a 3-ethylpyridine moiety in a monoterpenoid indole. The rhazinilam-type alkaloids (rhazinicine, nor-rhazinicine, rhazinal, and rhazinilam) showed strong cytotoxicity toward human KB, HCT-116, MDA-MB-231, and MRC-5 cells, while pneumatophorine, the uleine alkaloid undulifoline, and the strychnan alkaloids, N4-demethylalstogustine and echitamidine, induced concentration dependent relaxation in phenylephrine-precontracted rat aortic rings.

Topics: Aldehydes; Alkaloids; Alstonia; Animals; Antineoplastic Agents, Phytogenic; Aorta; Carbazoles; Cell Line, Tumor; Crystallography, X-Ray; Drug Evaluation, Preclinical; Heterocyclic Compounds, 4 or More Rings; Humans; Indole Alkaloids; Indolizines; Lactams; Molecular Structure; Phenylephrine; Pyrans; Pyridines; Rats; Secologanin Tryptamine Alkaloids; Vasodilator Agents