Cytotoxicity of endemic Haplophyllum megalanthum Bornm. and its newly isolated alkaloids and lignans

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemical Systematics and Ecology Pub Date : 2024-09-14 DOI:10.1016/j.bse.2024.104901
Serhat Demir , Malene Johanne Petersen , Louise Kjaerulff , Nehir Unver-Somer , Dan Staerk
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Abstract

In this study, two previously unreported lignans [4′-O-demetylsuchilactone-8′-ol (1), 7-O-(3-methyl-2,3-dihydroxy-butyl)isodaurinol] (2), four new alkaloids (haplomegalanthine (3), megalantin (4), megalanthamide (5), glycoisohaplopine (6) and thirty-five known compounds (7–41) were isolated from Haplophyllum megalanthum Bornm. (Rutaceae). Pinoresinol (23), epipinoresinol (24), indole-3-carbaldehyde (29), N-[2-(4-hydroxyphenyl)ethyl]-3-methylbut-2-enamide (34), 7,8-dimethoxyfuroquinoline-4-one (35), cis-khellactone (36), 4,4′-dihydroxy-3,3′,9-trimethoxy-9,9′-epoxylignan (37), ulopterol (39) and trans-decursidinol (40) were identified for the first time in the genus Haplophyllum. Also, 4′-O-demethylsuchilactone (16) and N-(4-hydroxyphenethyl)benzamide (32) were found for the first time within the family Rutaceae. Structures of the compounds were elucidated by the use of HRMS, UHPLC-MS and 1D/2D NMR analyses. Furthermore, cytotoxic activity of the crude extract and previously unreported compounds (1–3, 5, 6) on colon cancer cell line HT29 were tested by the MTT method. IC50 values were determined for these five compounds and the crude extract as 18.48 ± 0.94 μg/ml, 52.62 ± 7.27 μg/ml, 23.15 ± 6.70 μg/ml, 21.45 ± 2.48 μg/ml, 5.06 ± 0.19 μg/ml and 2.82 ± 0.012 μg/ml, respectively.

The present report is the first detailed phytochemical investigation of the title plant pointing out that it comprises a rich source of diverse chemical constituents including new compounds with promising cytotoxic activity.

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当地特有的 Haplophyllum megalanthum Bornm.及其新分离的生物碱和木脂素的细胞毒性
本研究从巨叶女贞中分离出两种以前未报道的木脂素[4′-O-去甲基水苏内酯-8′-醇(1)、7-O-(3-甲基-2,3-二羟基丁基)异贝壳杉醇](2)、四种新生物碱(haplomegalanthine(3)、megalantin(4)、megalanthamide(5)、glycoisohaplopine(6)和 35 种已知化合物(7-41)、从 Haplophyllum megalanthum Bornm.(芸香科)中分离出了四种新生物碱(haplomegalanthine (3)、megalantin (4)、megalanthamide (5)、glycoisohaplopine (6))和 35 种已知化合物 (7-41)。(芸香科)中分离出了 35 种已知化合物(7-41)。松脂醇(23)、表松脂醇(24)、吲哚-3-甲醛(29)、N-[2-(4-羟基苯基)乙基]-3-甲基丁-2-烯酰胺(34)、7,8-二甲氧基呋喃喹啉-4-酮(35)、顺式黄柏内酯(36)、4,4′-dihydroxy-3,3′,9-trimethoxy-9,9′-epoxylignan (37)、ulopterol (39) 和 trans-decursidinol (40)。此外,在芸香科植物中首次发现了 4′-O-去甲基水苏内酯(16)和 N-(4-羟基苯乙基)苯甲酰胺(32)。通过使用 HRMS、UHPLC-MS 和 1D/2D NMR 分析,阐明了这些化合物的结构。此外,还采用 MTT 法测试了粗提取物和以前未报道过的化合物(1-3、5、6)对结肠癌细胞株 HT29 的细胞毒性活性。这五种化合物和粗提取物的 IC50 值分别为 18.48 ± 0.94 μg/ml、52.62 ± 7.27 μg/ml、23.15 ± 6.70 μg/ml、21.45 ± 2.48 μg/ml、5.06 ± 0.19 μg/ml、2.82 ± 0.012 μg/ml。本报告是对标题植物进行的首次详细植物化学调查,指出该植物含有丰富的多种化学成分,包括具有良好细胞毒性活性的新化合物。
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来源期刊
Biochemical Systematics and Ecology
Biochemical Systematics and Ecology 生物-进化生物学
CiteScore
3.00
自引率
12.50%
发文量
147
审稿时长
43 days
期刊介绍: Biochemical Systematics and Ecology is devoted to the publication of original papers and reviews, both submitted and invited, in two subject areas: I) the application of biochemistry to problems relating to systematic biology of organisms (biochemical systematics); II) the role of biochemistry in interactions between organisms or between an organism and its environment (biochemical ecology). In the Biochemical Systematics subject area, comparative studies of the distribution of (secondary) metabolites within a wider taxon (e.g. genus or family) are welcome. Comparative studies, encompassing multiple accessions of each of the taxa within their distribution are particularly encouraged. Welcome are also studies combining classical chemosystematic studies (such as comparative HPLC-MS or GC-MS investigations) with (macro-) molecular phylogenetic studies. Studies that involve the comparative use of compounds to help differentiate among species such as adulterants or substitutes that illustrate the applied use of chemosystematics are welcome. In contrast, studies solely employing macromolecular phylogenetic techniques (gene sequences, RAPD studies etc.) will be considered out of scope. Discouraged are manuscripts that report known or new compounds from a single source taxon without addressing a systematic hypothesis. Also considered out of scope are studies using outdated and hard to reproduce macromolecular techniques such as RAPDs in combination with standard chemosystematic techniques such as GC-FID and GC-MS.
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