Yokohama City University, Seto 22-2, Kanazawa-ku, Yokohama 236-0027, Japan.
Faculty of Fisheries Sciences, Hokkaido University, Hakodate 041-8611, Japan.
J Nat Prod. 2021 Apr 23;84(4):1203-1209. doi: 10.1021/acs.jnatprod.0c01280. Epub 2021 Mar 31.
The structure of protoaculeine B, the N-terminal residue of the marine peptide toxin aculeine B, is revised to the -1,3-disubstituted tetrahydro-β-carboline framework. We prepared two truncated model compounds that lack a long-chain polyamine using the one-step Pictet-Spengler reaction of tryptophan and compared their NMR, mass spectra, and chemical reactivity with those of the natural protoaculeine B. The synthetic models reproduced the profiles of the natural product well, which confirmed the appropriateness of the structure revision.
原型芋螺毒素 B 的结构被修正为 -1,3-取代的四氢-β-咔啉骨架,原型芋螺毒素 B 是海洋肽毒素芋螺毒素 B 的 N 端残基。我们使用色氨酸的一步皮克特-斯宾格勒(Pictet-Spengler)反应制备了两个缺少长链多胺的截断模型化合物,并比较了它们的 NMR、质谱和化学反应性与天然原型芋螺毒素 B 的异同。合成模型很好地再现了天然产物的特征,这证实了结构修正的合理性。