Phytochemical screening, antiproliferative evaluation, and molecular docking studies of Acacia nilotica fruit from Nigeria

Q3 Physics and Astronomy Ecletica Quimica Pub Date : 2024-01-18 DOI:10.26850/1678-4618eq.v49.2024.e1512
William Ojoniko Anthony, E. O. Okpala, Kehinde Gabriel Obiyenwa, Godfrey Okechukwu Eneogwe, B. Semire
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Abstract

Acacia nilotica, (Fabaceae), is valued for its medicinal properties. We examine the antiproliferative properties of the aqueous fruit extract of A. nilotica. Aqueous extract from Acacia has been associated with potential anticancer effects in fruits and vegetables through screening, antiproliferative, and molecular docking evaluation. Phytochemical screening reveals the presence of alkaloids, saponins, tannins, flavonoids, steroids, and carbohydrates. The extracts showed significant antiproliferative effects at eight concentrations (8�50 mg�mL�1) examined in comparison to the standard (methotrexate). When compared to Sorghum bicolor seed radicles treated with methotrexate at 48, 72, and 96 h, 50 mg�mL�1 extract significantly inhibited the generation of seed radicals, with potent inhibitions of 87.06, 83.48, and 81.45%. Analysis of molecular docking results showed that [(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]3,4,5-trihydroxybenzoate (D21), (5R,9R,10R,13S,14S,17S)-17-[(2S,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one (D28) and [(2R,3S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate (D29) have strong tendency to inhibit dihydrofolate reductase (1VDR), capase-9 (6J15) and Mycobacterium tuberculosis (Mtb) (6J17) better than methotrexate and azacitidine, known antiproliferative drugs. These findings support the use of A. nilotica in traditional medicine for the treatment of tuberculosis and cancer.
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尼日利亚金合欢果实的植物化学筛选、抗增殖评价和分子对接研究
金合欢(豆科)因其药用价值而备受重视。我们研究了金合欢果实水提取物的抗增殖特性。通过筛选、抗增殖和分子对接评估,相思树的水提取物与水果和蔬菜的潜在抗癌作用有关。植物化学筛选显示了生物碱、皂苷、单宁、黄酮类、类固醇和碳水化合物的存在。与标准物质(甲氨蝶呤)相比,提取物在八个浓度(8.50 mg.mL.1)下均显示出明显的抗增殖作用。与甲氨蝶呤处理48、72和96小时后的高粱双色种子辐射体相比,50 mg.mL.1提取物可明显抑制种子自由基的生成,抑制率分别为87.06%、83.48%和81.45%。分子对接分析结果显示,[(2R,3S)-2-(3,4-二羟基苯基)-3,5-二羟基-3,4-二氢-2H-苯并吡喃-7-基]3,4,5-三羟基苯甲酸酯(D21)、(5R,9R,10R,13S,14S、17S)-17-[(2S,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one (D28) and [(2R,3S)-2-(3,4-二羟基苯基)-3,7-二羟基-3,4-二氢-2H-苯并吡喃-5-基] 3,4,5-三羟基苯甲酸酯(D29)对二氢叶酸还原酶(1VDR)、capase-9(6J15)和结核分枝杆菌(Mtb)(6J17)的抑制作用比已知的抗增殖药物甲氨蝶呤和阿扎胞苷更强。这些发现支持在传统医学中使用 A. nilotica 治疗结核病和癌症。
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来源期刊
Ecletica Quimica
Ecletica Quimica Chemistry-Chemistry (all)
CiteScore
1.70
自引率
0.00%
发文量
32
审稿时长
28 weeks
期刊最新文献
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