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首页> 外文期刊>Proceedings >Synthesis of Novel and Potential Antimicrobial, Antioxidant and Anticancer Chalcones and Dihydropyrazoles Bearing Isoxazole Scaffold
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Synthesis of Novel and Potential Antimicrobial, Antioxidant and Anticancer Chalcones and Dihydropyrazoles Bearing Isoxazole Scaffold

机译:合成新型和潜在抗微生物,抗氧化剂和抗癌杀铝和含二氢吡唑轴承的异恶唑支架

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摘要

A series of isoxazole based (E)-1-(isoxazole-5-yl)-3-(substituted phenyl)-prop-2-en-1-ones (chalcones, 3a-3o) and 3-(isoxazol-5-yl)-5-(substituted phenyl)-4,5-dihydro-1H-pyrazole-1-carboxamide (dihydropyrazoles, 4a-4o) were synthesized, characterized and evaluated for their antimicrobial, antioxidant and anticancer properties. Chalcones exhibited excellent antibacterial and antioxidant activities whereas the dihydropyrazoles shown superior antifungal and anticancer activities. The compound 3l containing 3,4,5-trimethoxy phenyl ring showed the potent antibacterial activity (MIC = 1 μg/mL) as well as the antioxidant activity (IC50 = 5 μg/mL) whereas the dihydropyrazole, 4o (MIC = 0.5 μg/mL) bearing the 2-chloro-3,4-dimethoxyphenyl was the potent antifungal compound identified. The dihydropyrazoles 4n and 4h possessing 2-fluoro-3,4-dimethoxyphenyl and 3,4-dimethoxyphenyl substituents exhibited potent anticancer activity against prostate cancer cell line (DU-145) with MIC 2 and 4 μg/mL respectively. The structure activity relationships had shown that there is a marked influence of both electron withdrawing halogens and electron releasing methoxyl groups on the above biological activities. All the compounds were evaluated for toxicity on normal human cell lines (LO2) and found to be non-toxic. These studies could help to synthesize, explore and identify new isoxazole containing leads for antimicrobial, antioxidant and anticancer properties.
机译:基于异恶唑的(E)-1-(异恶唑-5-基)-3-(取代的苯基)-1P-2-ZH-1-α(Chalcones,3A-3O)和3-(异恶唑-5-合成,合成了YL)-5-(取代的苯基)-4,5-二氢-1H-吡唑-1-甲酰胺(二氢吡唑,4A-40),其特征和评价其抗微生物,抗氧化剂和抗癌性。 Chalcones表现出优异的抗菌和抗氧化活性,而二氢吡嗪显示出优异的抗真菌和抗癌活性。含有3,4,5-三甲氧基苯基环的化合物3L显示有效的抗菌活性(MIC =1μg/ mL)以及抗氧化活性(IC50 =5μg/ mL),而二氢吡唑,4O(MIC =0.5μg / ml)载有2-氯-3,4-二甲氧基苯基是鉴定的有效的抗真菌化合物。具有2-氟-3,4-二甲氧基苯基和3,4-二甲氧基苯基取代基的二氢吡唑4N和4H分别表现出与麦克风2和4μg/ mL的前列腺癌细胞系(DU-145)的有效抗癌活性。结构活性关系表明,电子吸附卤素和电子释放甲氧基对上述生物活性有明显影响。在正常人体细胞系(LO2)上对所有化合物进行毒性进行评估,发现无毒。这些研究可以帮助合成,探索和鉴定含有抗微生物,抗氧化和抗癌性质的新的异恶唑。

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