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首页> 外文期刊>Asian journal of research in chemistry >Docking Studies and Synthesis of Novel Flavones Screened for Biological Activities like Anticancer and Antioxidant Activity
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Docking Studies and Synthesis of Novel Flavones Screened for Biological Activities like Anticancer and Antioxidant Activity

机译:筛选抗生物活性如抗癌和抗氧化活性的新型黄酮的对接研究和合成

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摘要

Flavones are the derivatives of flavonoids, possessing the wider range of biological ac'ions. A novel series of flavonoid Derivatives with the help of substituted benzaldehyde were synthesized and screened for biological activities like anticancer and antioxidant activity. All synthesized derivatives were, creened for in-vitro cytotoxicity by Brine shrimp lethality assay in which l-(2, 4-dihydroxyphenyl)-3-(4-(dimethyl amino) phenyl) prop-2ene-lone.(MCR-001) and 2-(4-(Di-methylamino) phenyl)-7-hydroxy-4-H-cbromen-4-one. (MCR-002), 2-hydroxy-2-(4-(methyl (4-nitrostyryl) amino) phenyl)-4-oxochroman-7-yl benzoate. (MCR-004) and 2-(4-dimethyl amino) phenyi)-4-oxo-4H-chromen-7-yl benzoate. (MCR-005) showed highest anticancer activity as compared to 5-fluorouracil due to presence of hydroxy group. Among synthesized compounds, 4-nitro flavonoids compound derivatives were screened for antioxidant activity by using DPPH Scavenging Method. 2-(4-dimethyl amino) phenyl)-2-hydroxy 4-oxochroman-6-yl benzoate (MCR-005) showed highest antioxidant activity as compared to ascorbic acid. This work has revealed the scope and potential of flavonoids for future exploration to synthesize substituted flavonoids and chalcone derivatives by the use of different substituted benzaldehyde.
机译:黄酮是类黄酮的衍生物,具有更广泛的生物活性。合成了一系列新的类黄酮衍生物,其具有取代的苯甲醛,并针对其生物活性如抗癌和抗氧化活性进行了筛选。通过盐水虾的致死性测定法对所有合成的衍生物进行体外细胞毒性处理,其中1-(2,4-二羟基苯基)-3-(4-(二甲基氨基)苯基)丙-2-烯-酮(MCR-001)和2-(4-(二-甲基氨基)苯基)-7-羟基-4-H-丁烯-4-。 (MCR-002),2-羟基-2-(4-(甲基(4-硝基苯乙烯基)氨基)苯基)-4-氧代苯并吡喃-7-苯甲酸酯。 (MCR-004)和2-(4-二甲基氨基)苯基)-4-氧代-4H-铬基-7-苯甲酸酯。 (MCR-005)由于存在羟基,因此与5-氟尿嘧啶相比具有最高的抗癌活性。在合成的化合物中,使用DPPH清除方法筛选了4-硝基类黄酮化合物衍生物的抗氧化活性。与抗坏血酸相比,2-(4-二甲基氨基)苯基)-2-羟基4-氧代苯并六基苯甲酸酯(MCR-005)具有最高的抗氧化活性。这项工作揭示了黄酮类化合物的范围和潜力,以供将来探索通过使用不同的取代苯甲醛合成取代的黄酮类和查尔酮衍生物。

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