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Photocatalyzed Chemo-Selective Alkylation of Quinones and Phenothiazinones with Alkyl Amides: Photophysical and Cytotoxic Activity Studies

机译:喹酮酮和苯噻嗪酮与烷基酰胺的光催化化学选择性烷基化:光学和细胞毒性活性研究

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Alkylation of naphthoquinones (NQs) and phenothiazinone (PTZs) was achieved through chemo-selective functionalization of different mono/di-alkyl amides in the presence of photo- catalyst eosin-y and TBHP under the influence of blue light (Blue LEDs) as an energy source, at room temperature to get the products in moderate to good yield. These highly conjugated alkylated compounds displays absorption and emission in the visible region, has potential to be used as fluorescent probes and other light harvesting materials. Insilico study revealed that some of these compounds are potential phosphodiesterase-4B (PDE4B) inhibitors and has excellent drug like properties. Furthermore, the cytotoxic activity of alkylated quinones toward human lung cancer cell line (A549) was studied.
机译:萘喹酮(NQS)和苯噻嗪酮(PTZ)的烷基化是通过在光催化剂eosin-Y和TBHP的情况下通过化学选择性官能化在蓝光(蓝色LED)的影响下实现的 能源,在室温下以中等至良好的收率使产品。 这些高度共轭的烷基化化合物显示可见区域的吸收和发射,有可能用作荧光探针和其他光收集材料。 Insilico研究表明,其中一些化合物是潜在的磷酸二酯酶4B(PDE4B)抑制剂,并且具有出色的药物。 此外,研究了烷基化奎因酮对人肺癌细胞系(A549)的细胞毒性活性。

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