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Anti-Inflammatory,Antiallergic and COVID-19 Main Protease(M~(pro))Inhibitory Activities of Butenolides from a Marine-Derived Fungus Aspergillus costaricaensis

机译:抗炎,抗乳糖和covid-19主要蛋白酶(M〜(Pro))抑制丁乙酰亚胺的抑制作用,来自海洋衍生的真菌costaricaensis

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Amid the current COVID-19 pandemic,the emergence of several variants in a relatively high mutation rate(twice per month)strengthened the importance of finding out a chemical entity that can be potential for developing an effective medicine.In this study,we explored ethyl acetate(EtOAc)extract of a marine-derived fungus Aspergillus cosatricaensis afforded three butenolide derivatives,butyrolactones I,VI and V(1-3),two naphtho-γ-pyrones,TMC-256 A1(4)and rubrofusarin B(5)and methyl p-hydroxyphenyl acetate(6).Structure identification was unambiguously determined based on exhaustive spectral analyses including 1D/2DNMR and mass spectrometry.The isolated compounds(1-6)were assessed for their in vitro anti-inflammatory,antiallergic,elastase inhibitory activities and in silico SARS-CoV-2 main protease(M~(pro)).Results exhibited that only butenolides(1 and 2)revealed potent activities similar to or more than reference drugs unlike butyrolactone V(3)suggesting them as plausible chemical entities for developing lead molecules.
机译:在当前的COVID-19大流行中,几种变体以相对较高的突变率(每月两次)的出现增强了发现可以开发有效药物的化学实体的重要性。在这项研究中,我们探索了乙基乙酸盐(ETOAC)提取物的海洋衍生真菌曲霉菌cosatricaensis提供了三个丁烯衍生物,丁酰乳酮I,VI和V(1-3),两个NAPHTHO-γ-吡喃,TMC-256 A1(4)和Rubrofusarin b(5)基于详尽的光谱分析(包括1D/2DNMR和质谱法),明确确定了结构鉴定的结构鉴定。分离的化合物(1-6)的体外抗抗抗激素,抗抑制剂,抗抗激素,抗激弹性,抗激弹性,抗激弹性,抗激弹性,活动和硅sar-cov-2主要蛋白酶(M〜(pro))。结果表明,只有丁烯酰基(1和2)揭示了与参考药物相似或超过参考药物的有效活性,与丁蜜酮V(3)不同,这表明它们是合理的化学物质实体用于开发铅分子。

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