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从 中分离并鉴定具有广泛药用价值的分子,并评估其对人癌细胞系的细胞毒性活性。

Isolation and characterisation of pharmaceutically versatile molecules from and evaluation of their cytotoxic activity against human cancer cell lines.

机构信息

Plant Molecular Biology and Biotechnology Division, CSIR-Indian Institute of Integrative Medicine, Sanatnagar, Srinagar, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, Uttar Pradesh, India.

出版信息

Nat Prod Res. 2023 Mar;37(5):857-862. doi: 10.1080/14786419.2022.2092864. Epub 2022 Jun 24.

Abstract

The disclosed study reveals isolation, characterization and anticancer evaluation of . The extracts and isolated compounds were used for cytotoxic activity against (lung (A549), pancreatic (MIAPaCa), colon (HCT-116), breast (MDA-MB-231) and breast (MDA-MB-468) cell lines. The extracts were screened for cytotoxicity using MTT colorimetric assay. Out of all extracts, methanolic (30) %: chloroform fraction (TAW6) with 75.01% inhibition at a concentration 100 µg/mL was observed. The selected extracts were further processed for column chromatography and led to isolation of seven compounds (A to G). The structural determination of isolated compounds was carried out using HNMR, CNMR, IR and HRMS. All the isolates were tested for cytotoxic activity and compound B was found most active with IC values 11.29 µg against HCT-116 (Colon). The compound B was then used for detailed study via and . Thus the significant anticancer activity particularly against colon cancerous cell lines recommends that the ( could act as a potential drug candidate for cancer, more particularly for colon cancer.

摘要

本研究揭示了 的分离、鉴定和抗癌活性评价。提取物和分离得到的化合物被用于对(肺癌(A549)、胰腺(MIAPaCa)、结肠(HCT-116)、乳腺(MDA-MB-231)和乳腺(MDA-MB-468)细胞系)的细胞毒性活性进行检测。采用 MTT 比色法对提取物进行了细胞毒性筛选。在所有提取物中,观察到浓度为 100μg/mL 时,甲醇(30%):氯仿部分(TAW6)的抑制率为 75.01%。选择的提取物进一步进行柱色谱分离,得到了七种化合物(A 至 G)。通过 HNMR、CNMR、IR 和 HRMS 确定了分离化合物的结构。所有分离得到的化合物均进行了细胞毒性活性测试,结果发现化合物 B 对 HCT-116(结肠)的 IC 值为 11.29μg,具有最强的活性。然后,通过 和 对化合物 B 进行了详细研究。因此,特别是对结肠癌细胞系的显著抗癌活性表明, 可能成为癌症的潜在药物候选物,特别是结肠癌。

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