AI Article Synopsis

  • Nine new monoterpene indole alkaloids, named rauvomitorine A-I, were discovered in Rauvolfia vomitoria, including unique structural types that hadn’t been identified before.
  • Extensive analysis techniques like spectroscopy and X-ray diffraction were used to determine their structures, particularly highlighting rauvomitorine A, which features a novel alkaloid framework.
  • The study evaluated the isolated alkaloids for their potential as acetylcholinesterase inhibitors, revealing some to have promising activity against cancer cell lines, especially noting the importance of suaveoline-type alkaloids in this area for possible drug development.

Article Abstract

Nine undescribed monoterpene indole alkaloids, rauvomitorine A-I, including an unprecedented C-9-methoxymethylene-sarpagine framework alkaloid, two rare suaveoline framework type alkaloids, and six yohimbine framework type alkaloids, as well as eleven known alkaloids, were isolated from the stems of Rauvolfia vomitoria Afzel. (Apocynaceae). The structures of the unreported alkaloids were elucidated by extensive spectroscopic analysis and single-crystal X-ray diffraction analysis with Cu Kα radiation. Rauvomitorine A with an unreported framework type represents the first example of C-9-methoxymethylene-sarpagine alkaloids and its plausible biosynthetic pathway was proposed. All the isolated alkaloids were evaluated their acetylcholinesterase inhibitory (AChE) activities and cytotoxicity against five cancer cell lines and some of them exhibited potential anti-AChE activities with IC values ranging from 49.76 to 186.62 μM. Importantly, this is the first report of the AChE inhibitory activities on suaveoline framework type alkaloids, suggesting this type of alkaloids may be valuable sources for the discovery of AChE inhibitory agents. A preliminary structure-activity relationship for AChE inhibitory activities of the isolated alkaloids is also discussed, providing some clues to designing lead compounds for AChE inhibitors.

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http://dx.doi.org/10.1016/j.phytochem.2020.112450DOI Listing

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