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评价 1,3-噁唑-4-基磷盐的体外抗癌活性。

Evaluation of Anticancer Activity of 1,3-Oxazol-4-ylphosphonium Salts in Vitro.

机构信息

Department of Chemistry of Bioactive Nitrogen-Containing Heterocyclic Bases, V. P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, Murmanska st. 1, 02094, Kyiv, Ukraine.

Laboratoire COBRA, INSA Rouen Normandie, Bâtiment IRCOF, rue Tesnière 1, 76821, Mont Saint-Aignan Cedex, France.

出版信息

ChemMedChem. 2022 Oct 19;17(20):e202200319. doi: 10.1002/cmdc.202200319. Epub 2022 Sep 15.

Abstract

A novel series of 1,3-oxazol-4-yltriphenylphosphonium salts has been synthesized and functionalized. Oxazole derivatives were subjected to NCI in vitro assessment. Seven most active derivatives have been selected for five-dose assay. Among them, compounds 9 ([2-(4-methylphenyl)-5-[(4-methylphenyl)sulfanyl]-1,3-oxazol-4-yl]triphenylphosphonium perchlorate), 1 ([5-(4-methylphenyl)amino]-2-phenyl-1,3-oxazol-4-yl]triphenylphosphonium perchlorate) and 4 ([5-phenyl-2-[(4-methylphenyl)amino]-1,3-oxazol-4-yl]triphenylphosphonium perchlorate) were the most active against all tested cancer subpanels. Statistical analysis of the total panel data showed average values of parameters of anticancer activity in the range of 0.3-1.1 μM (GI ), 1.2-2.5 μM (TGI) and 5-6 μM (LC ). It was found that the presence of phenyl or 4-methylphenyl groups at C(2) and C(5) in the oxazole ring is of critical importance for the manifestation of the anticancer activity. Matrix COMPARE analysis using LC vector showed a high positive correlation of compound 9 with standard anticancer agents that can directly disrupt mitochondrial function, causing programmed death of cancer cells. The obtained results indicate the anticancer activity of 1,3-oxazol-4-ylphosphonium salts, which could be useful for developing new anticancer drugs. The most active of them can be recommended for further in-depth studies and synthesis of new derivatives with antitumor activity on their basis.

摘要

一种新型的 1,3-恶唑-4-基三苯基膦盐系列已被合成并官能化。恶唑衍生物进行了 NCI 体外评估。选择了七种最活跃的衍生物进行五剂量测定。其中,化合物 9([2-(4-甲基苯基)-5-[(4-甲基苯基)硫基]-1,3-恶唑-4-基]三苯基膦高氯酸盐)、1([5-(4-甲基苯基)氨基]-2-苯基-1,3-恶唑-4-基]三苯基膦高氯酸盐)和 4([5-苯基-2-[(4-甲基苯基)氨基]-1,3-恶唑-4-基]三苯基膦高氯酸盐)对所有测试的癌症亚群最具活性。对总面板数据的统计分析表明,抗癌活性参数的平均值在 0.3-1.1μM(GI)、1.2-2.5μM(TGI)和 5-6μM(LC)范围内。结果发现,恶唑环的 C(2)和 C(5)位上的苯基或 4-甲基苯基的存在对表现抗癌活性具有重要意义。使用 LC 向量的 COMPARE 矩阵分析显示,化合物 9 与可直接破坏线粒体功能、导致癌细胞程序性死亡的标准抗癌药物具有高度正相关。研究结果表明,1,3-恶唑-4-基膦盐具有抗癌活性,可用于开发新的抗癌药物。其中最活跃的可以推荐进一步深入研究,并在此基础上合成具有抗肿瘤活性的新衍生物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e561/9825890/05d896a006d4/CMDC-17-0-g004.jpg

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