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合成新型吡唑酮候选物及其部分生物活性和计算机模拟研究。

Synthesis of novel pyrazolone candidates with studying some biological activities and in-silico studies.

机构信息

Department of Chemistry, Sciences College, Taif University, P. O. Box 11099, 21944, Taif, Saudi Arabia.

Department of Chemistry, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt.

出版信息

Sci Rep. 2023 Nov 6;13(1):19170. doi: 10.1038/s41598-023-43575-z.

Abstract

Pyranopyrazole derivatives have a vital role in the class of organic compounds because of their broad spectrum of biological and pharmacological importance. Our current goal is the [3 + 3] cycloaddition of benzoyl isothiocyanate and pyrazolone 1 to undergo oxidation cyclization, producing pyrazoloxadiazine 3. The diol 5 was obtained as a condensation of two equivalents of 1 with thiophene-2-carboxaldehyde in acetic acid above the sodium acetate mixture. When the condensation was carried out in piperidine under fusion, unsaturated ketone 4 was obtained. The pyrazolo pyran derivative 11 resulted from the [3 + 3] cycloaddition of 1 and cinnamic acid, while the Pyrone derivative was prepared by acylation of 12 with two equivalents of acetic anhydride. Phthalic anhydride undergoes arylation using zinc chloride as a catalyst. The cyclic keto acid 23 was synthesized by the action of succinic anhydride on 12 in the acetic medium, while the latter reacted with cinnamic acid, leading to pyrazole derivative 24. All of these reactions were through the Michael reaction mechanism. All the tested compounds showed good antimicrobial activity against pathogenic microorganisms; newly synthesized compounds were also screened for their antioxidant activity. Rational studies were carried out by the ABTs method to allow a broader choice of activities. In addition, similar off-compounds were conducted. Molecular docking studies with the CB-Dock server and MD simulations were created with the default settings of the Solution Builder on the CHARMM-GUI server at 150 nm. A good correlation was obtained between the experimental results and the theoretical bioavailability predictions using POM theory.

摘要

吡喃并吡唑衍生物因其广泛的生物和药理重要性而在有机化合物类别中具有重要作用。我们目前的目标是苯甲酰异硫氰酸酯和吡唑酮 1 的[3+3]环加成经历氧化环化,生成吡唑并噁二嗪 3。二醇 5 是通过在乙酸中用噻吩-2-甲醛与 1 的两个当量缩合得到的,混合物上面是乙酸钠。当在哌啶中进行缩合时,得到不饱和酮 4。吡唑并吡喃衍生物 11 是由 1 和肉桂酸的[3+3]环加成得到的,而吡喃酮衍生物是通过 12 与两当量的乙酸酐酰化得到的。邻苯二甲酸酐在氯化锌作为催化剂的作用下发生芳基化反应。环状酮酸 23 是通过琥珀酸酐在乙酸介质中作用于 12 合成的,而后者与肉桂酸反应,生成吡唑衍生物 24。所有这些反应都是通过迈克尔反应机制进行的。所有测试的化合物对致病微生物都表现出良好的抗菌活性;新合成的化合物也被筛选其抗氧化活性。通过 ABTs 方法进行了合理的研究,以允许更广泛的选择活性。此外,还进行了类似的脱化合物研究。使用 CHARMM-GUI 服务器上的 Solution Builder 以默认设置创建了与 CB-Dock 服务器的分子对接研究和 MD 模拟。使用 POM 理论,实验结果与理论生物利用度预测之间得到了很好的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0406/10628256/ee11d6e102ee/41598_2023_43575_Fig1_HTML.jpg

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