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翠雀素-P 辅助十 decenol 作为潜在的抗癌剂:其分离、表征和验证。

Tragia plukenetii-Assisted Omega-Decenol as Potential Anticancer Agent: its Isolation, Characterization, and Validation.

机构信息

Department of Biotechnology, Karpagam Academy of Higher Education, Coimbatore, Tamil Nadu, India.

出版信息

Appl Biochem Biotechnol. 2023 Mar;195(3):1699-1722. doi: 10.1007/s12010-022-04221-y. Epub 2022 Nov 11.

Abstract

The second most common and lethal disease is lung cancer. To combat the negative effects of today's synthetic medications, natural phytomedicines are required. Tragia plukenetii is a medicinal plant native to India that belongs to the Euphorbiaceae family. The purpose of this research is to isolate bioactive compounds from T. plukenetii leaves and then test them for anticancer property. A single compound (CH: ME-20:80) was separated using TLC, and an RF value of 0.55 was determined. Spectral analyses utilizing UV-Visible Spectrophotometer and FT-IR were used to examine the absorbance and functional groups. C-NMR and H-NMR studies revealed the tentative name of the purified phytochemical as omega-decenol (OD). Further antioxidant and anticancer properties of OD were tested for in vitro. In comparison to conventional L-ascorbic acid, the DPPH radical scavenging assay experiment yielded an IC of 147.48 g/ml. With an IC value of 24 µg/ml (Omega-decenol) and 32 µg/ml (doxorubicin), the MTT assay demonstrated the cytotoxic capability against the A549 lung cancer cell line. FACS revealed the cell cycle arrest of A549 at S phase compared to control with the high-dose IC (250 µg/ml) of omega-decenol. Twelve major compounds were detected in the active fraction using GC-MS analysis, where n-hexadecanoic acid was found as a major. Omega-decenol showed good binding affinity against EGFR, amongst other receptors in the in silico docking study. This research reveals the potent anticancer activity of the isolated compound omega-decenol from T. plukenetii leaves and provides a key path to understanding the molecular interaction in anticancer aspects against adenocarcinoma.

摘要

第二种最常见和致命的疾病是肺癌。为了对抗当今合成药物的负面影响,需要天然植物药。 Tragia plukenetii 是一种原产于印度的药用植物,属于大戟科。本研究的目的是从 T. plukenetii 叶中分离出生物活性化合物,然后测试其抗癌特性。利用 TLC 分离出一种单一化合物(CH:ME-20:80),并确定其 RF 值为 0.55。利用紫外可见分光光度计和傅里叶变换红外光谱对光谱进行分析,以检查吸光度和官能团。 C-NMR 和 H-NMR 研究表明,纯化植物化学物质的暂定名为ω-癸烯醇(OD)。进一步测试了 OD 的体外抗氧化和抗癌特性。与传统的 L-抗坏血酸相比,DPPH 自由基清除实验的 IC 为 147.48 g/ml。OD 对 A549 肺癌细胞系的细胞毒性作用的 MTT 试验的 IC 值为 24 µg/ml(ω-癸烯醇)和 32 µg/ml(阿霉素)。与对照相比,FACS 显示 A549 细胞在 S 期的细胞周期停滞,高剂量 IC(250 µg/ml)的 ω-癸烯醇。GC-MS 分析在活性部分检测到 12 种主要化合物,其中发现 n-十六烷酸为主要化合物。在计算机对接研究中,ω-癸烯醇对 EGFR 等其他受体表现出良好的结合亲和力。这项研究揭示了从 T. plukenetii 叶中分离出的化合物 ω-癸烯醇的强大抗癌活性,并为理解抗癌方面针对腺癌的分子相互作用提供了关键途径。

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