Isolation of 5-hydroxy-7-methoxy-8-O-β-D-glucopyranosyl-2S-flavanone from a new source, Haplanthodes tentaculatus: characterization and anticancer activity.

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Parth B Trivedi, Madhavi Badole
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引用次数: 0

Abstract

This study explores the anticancer properties of Haplanthodes tentaculatus, a plant indigenous to the Western Ghats of India. We isolated and characterised 5-hydroxy-7-methoxy-8-O-β-D-glucopyranosyl-2S-flavanone from H. tentaculatus, previously unreported in this plant, using preparative HPLC, NMR, and HRMS techniques. The compound's molecular structure and purity were confirmed, and its biological activity was evaluated on the MDA-MB-231 breast cancer cell line using the MTT assay. The compound exhibited notable cytotoxic effects with an IC50 value of 155.21 ± 1.59 sM. This work validates the therapeutic capabilities of H. tentaculatus and contributes to ongoing research on natural substances for anticancer drug development. The results suggest that H. tentaculatus could be a promising source of bioactive compounds, opening new possibilities for cancer therapy approaches.

从一种新资源 Haplanthodes tentaculatus 中分离出 5-hydroxy-7-methoxy-8-O-β-D-glucopyranosyl-2S-flavanone: 特征和抗癌活性。
本研究探讨了印度西高止山脉土生植物 Haplanthodes tentaculatus 的抗癌特性。我们采用制备型 HPLC、NMR 和 HRMS 技术,从 Haplanthodes tentaculatus 中分离并鉴定了 5-羟基-7-甲氧基-8-O-β-D-吡喃葡萄糖基-2S-黄烷酮。确认了该化合物的分子结构和纯度,并使用 MTT 法评估了其对 MDA-MB-231 乳腺癌细胞系的生物活性。该化合物具有显著的细胞毒性作用,其 IC50 值为 155.21 ± 1.59 sM。这项工作验证了 H. tentaculatus 的治疗能力,并为正在进行的抗癌药物开发天然物质研究做出了贡献。研究结果表明,H. tentaculatus 可能是一种有前景的生物活性化合物来源,为癌症治疗方法开辟了新的可能性。
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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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