Alstoboonine, an Ulean-Type Indole Alkaloid from Alstonia boonei Leaves

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Manuel Grimm, Ramona Börner, John N. Addotey, Thomas J. Schmidt and Verena Spiegler*, 
{"title":"Alstoboonine, an Ulean-Type Indole Alkaloid from Alstonia boonei Leaves","authors":"Manuel Grimm,&nbsp;Ramona Börner,&nbsp;John N. Addotey,&nbsp;Thomas J. Schmidt and Verena Spiegler*,&nbsp;","doi":"10.1021/acs.jnatprod.3c00832","DOIUrl":null,"url":null,"abstract":"<p ><i>Alstonia boonei</i> De Wild is a common plant in West Africa used in traditional medicine for various indications. While the stem bark has frequently been investigated, not much is known about the phytochemistry and bioactivity of the leaves. Within the current study, the major alkaloids of a hydroethanolic leaf extract were therefore isolated and characterized by MS, NMR, and ECD. This led to the identification of alstoboonine <b>1</b>, a new ulean-type alkaloid, along with eight previously reported indole alkaloids, 15-hydroxyangustilobine A (<b>2</b>), 6,7-seco-angustilobine B (<b>3</b>), 6,7-seco-19,20-α-epoxyangustilobine B (<b>4</b>), alstrostine E (<b>5</b>), alstrostine C (<b>6</b>), alstrostine D (<b>7</b>), 12-methoxyechitamidine (<b>8</b>), and 19-oxo-12-methoxyechitamidine (<b>9</b>). <b>1</b> was moderately active <i>in vitro</i> against <i>Plasmodium falciparum</i> NF54 (IC<sub>50</sub> 6.9 μM), but inactive against other protozoan parasites (<i>Trypanosoma brucei</i>, <i>Trypanosoma cruzi</i>, <i>Leishmania donovani</i>). No significant cytotoxic effects were observed in L6 rat skeletal myoblast cells and MCF-7 breast cancer cells. Similarly, compounds <b>3</b> to <b>9</b> did not show cytotoxicity in MCF-7 cells. Due to the reported traditional use of the plant as an anthelmintic, the major alkaloids <b>2</b>, <b>5</b>, <b>6</b>, and <b>8</b> were tested against the nematode <i>Caenorhabditis elegans</i>. Nematicidal effects were observed for <b>6</b> (LC<sub>50</sub> 400 μM), whereas <b>2</b>, <b>5</b>, and <b>8</b> were inactive.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"87 3","pages":"514–519"},"PeriodicalIF":3.3000,"publicationDate":"2023-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.3c00832","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Alstonia boonei De Wild is a common plant in West Africa used in traditional medicine for various indications. While the stem bark has frequently been investigated, not much is known about the phytochemistry and bioactivity of the leaves. Within the current study, the major alkaloids of a hydroethanolic leaf extract were therefore isolated and characterized by MS, NMR, and ECD. This led to the identification of alstoboonine 1, a new ulean-type alkaloid, along with eight previously reported indole alkaloids, 15-hydroxyangustilobine A (2), 6,7-seco-angustilobine B (3), 6,7-seco-19,20-α-epoxyangustilobine B (4), alstrostine E (5), alstrostine C (6), alstrostine D (7), 12-methoxyechitamidine (8), and 19-oxo-12-methoxyechitamidine (9). 1 was moderately active in vitro against Plasmodium falciparum NF54 (IC50 6.9 μM), but inactive against other protozoan parasites (Trypanosoma brucei, Trypanosoma cruzi, Leishmania donovani). No significant cytotoxic effects were observed in L6 rat skeletal myoblast cells and MCF-7 breast cancer cells. Similarly, compounds 3 to 9 did not show cytotoxicity in MCF-7 cells. Due to the reported traditional use of the plant as an anthelmintic, the major alkaloids 2, 5, 6, and 8 were tested against the nematode Caenorhabditis elegans. Nematicidal effects were observed for 6 (LC50 400 μM), whereas 2, 5, and 8 were inactive.

Abstract Image

Abstract Image

Alstobounine,一种产于Alstonia boonei叶中的Ulean型吲哚生物碱。
野生Alstonia boonei De Wild是西非的一种常见植物,用于各种适应症的传统医学。虽然人们经常对茎皮进行研究,但对叶的植物化学和生物活性知之甚少。因此,在目前的研究中,水乙醇叶提取物的主要生物碱被分离出来,并通过MS、NMR和ECD进行了表征。这导致鉴定了一种新的ulean型生物碱alstobounine 1,以及8种先前报道的吲哚生物碱,15-羟基angustilobine a(2)、6,7-seco-Angustilabine B(3)、6,7-seco-19,20-α-环氧Angustilbine B(4)、alstrostine E(5)、alstrastine C(6)、alstrustine D(7)、12-甲氧基针纺织品胺(8)和19-氧代-12-甲氧基针纺织品胺(9)。1在体外对恶性疟原虫NF54具有中等活性(IC50 6.9μM),但对其他原生动物寄生虫(布鲁氏锥虫、克鲁兹锥虫、杜氏利什曼原虫)没有活性。在L6大鼠骨骼成肌细胞和MCF-7乳腺癌症细胞中未观察到显著的细胞毒性作用。类似地,化合物3至9在MCF-7细胞中没有显示出细胞毒性。由于报道了该植物作为驱虫剂的传统用途,主要生物碱2、5、6和8对线虫秀丽隐杆线虫进行了测试。观察到6个(LC50 400μM)的杀线虫作用,而2、5和8个没有活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信