The isolation of novel pregnane steroids from Aglaia pachyphylla Miq. and the cytotoxicity against breast cancer cell lines (MCF-7)

从厚叶米仔兰中分离新型孕烷类固醇及其对乳腺癌细胞系(MCF-7)的细胞毒性

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作者:Wahyu Safriansyah, Siska Elisahbet Sinaga, Rustaman, Kindi Farabi, Mohamad Nurul Azmi, Rani Maharani, Nurlelasari, Unang Supratman, Sofa Fajriah, Desi Harneti

Abstract

Steroid groups isolated from many plants are known to play a significant role in various biological systems. Therefore, this research aimed to analyze two novel pregnane steroids, pachylenone A (1) and pachylenone B (2), isolated from Aglaia pachyphylla Miq. The cytotoxicity of the steroids was evaluated against MCF-7 breast cancer cell lines with other known steroid compounds, namely 5α-dihydroprogesterone (3), GSD-8 (4), trans-5α-pregn-l7(20)-en-3,16-dion (5), 20β-hydroxy-5αH-pregnan-3-one (6), 3β-hydroxy-5α-pregnan-20-one (7), aglaiasterol B (8), and 2β,3β-dihydroxypregnan-16-one (9). Meanwhile, structural elucidation was achieved through different spectroscopic methods including one and two-dimensional NMR, as well as mass spectroscopy and quantum chemical calculations (TD-DFT and NMR DP4+ probability). The cytotoxic effects of steroid compounds (1-9) on MCF-7 lines were also examined. The results showed that compound 8 had the strongest activity with an IC50 value of 228 μM, followed by compound 6 (IC50 568,76 μM), and pachylenone A (1) (IC50 768.73 μM). As a recommendation for future research, other activities of these compounds should be evaluated.

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