Avdović Edina H, Milanović Žiko, Simijonović Dušica, Antonijević Marko, Milutinović Milena, Nikodijević Danijela, Filipović Nenad, Marković Zoran, Vojinović Radiša
Department of Science, Institute for Information Technologies, University of Kragujevac, Jovana Cvijića bb, 34000 Kragujevac, Serbia.
Department of Biology and Ecology, Faculty of Science, University of Kragujevac, Radoja Domanovića 12, 34000 Kragujevac, Serbia.
Antioxidants (Basel). 2023 Dec 1;12(12):2070. doi: 10.3390/antiox12122070.
In this study, green synthesis of two derivatives of coumarin-hydroxybenzohydrazide, ()-2,4-dioxo-3-(1-(2-(2,3,4-trihydroxybenzoyl)hydrazyl)ethylidene)-chroman-7-yl acetate (), and ()-2,4-dioxo-3-(1-(2-(3,4,5-trihydroxybenzoyl)hydrazyl)ethylidene)chroman-7-yl acetate () is reported. Using vinegar and ethanol as a catalyst and solvent, the reactions were carried out between 3-acetyl-4-hydroxy-coumarin acetate and corresponding trihydroxybenzoyl hydrazide. The antioxidant potential of these compounds was investigated using the DPPH and ABTS assays, as well as the FRAP test. The obtained results reveal that even at very low concentrations, these compounds show excellent radical scavenging potential. The IC values for C-HB and C-HB in relation to the DPPH radical are 6.4 and 2.5 μM, respectively, while they are 4.5 and 2.0 μM in relation to the ABTS radical. These compounds have antioxidant activity that is comparable to well-known antioxidants such as gallic acid, NDGA, and trolox. These results are in good correlation with theoretical parameters describing these reactions. Moreover, it was found that inhibition of DPPH follows HAT, while inactivation of ABTS follows SET-PT and HAT mechanisms. Additionally, coumarin-hydroxybenzohydrazide derivatives induced moderate cytotoxic activity and show significant potential to modulate redox status in HCT-116 colorectal cancer cells. The cytotoxicity was achieved via their prooxidative activity and ability to induce oxidative stress in cancer cells by increasing O˙ concentrations, indicated by increased MDA and GSH levels. Thus, ROS manipulation can be a potential target for cancer therapies by coumarins, as cancer cells possess an altered redox balance in comparison to normal cells. According to the ADMET analysis, the compounds investigated show good pharmacokinetic and toxicological profiles similar to vitamin C and gallic acid, which makes them good candidates for application in various fields of industry and medicine.
在本研究中,报道了香豆素 - 羟基苯甲酰肼的两种衍生物,即()-2,4 - 二氧代 - 3 - (1 - (2 - (2,3,4 - 三羟基苯甲酰基)肼基)亚乙基) - 色满 - 7 - 基乙酸酯()和()-2,4 - 二氧代 - 3 - (1 - (2 - (3,4,5 - 三羟基苯甲酰基)肼基)亚乙基)色满 - 7 - 基乙酸酯()的绿色合成。以醋和乙醇作为催化剂和溶剂,使3 - 乙酰基 - 4 - 羟基香豆素乙酸酯与相应的三羟基苯甲酰肼进行反应。使用DPPH和ABTS测定法以及FRAP试验研究了这些化合物的抗氧化潜力。所得结果表明,即使在非常低的浓度下,这些化合物也表现出优异的自由基清除潜力。C - HB和C - HB相对于DPPH自由基的IC值分别为6.4和2.5 μM,而相对于ABTS自由基的IC值分别为4.5和2.0 μM。这些化合物具有与没食子酸、去甲二氢愈创木酸和生育酚类似物等知名抗氧化剂相当的抗氧化活性。这些结果与描述这些反应的理论参数具有良好的相关性。此外,发现对DPPH的抑制遵循氢原子转移(HAT),而对ABTS的失活遵循单电子转移 - 质子转移(SET - PT)和氢原子转移机制。此外,香豆素 - 羟基苯甲酰肼衍生物诱导了适度的细胞毒性活性,并显示出在HCT - 116结肠癌细胞中调节氧化还原状态的显著潜力。细胞毒性是通过它们的促氧化活性以及通过增加O˙浓度在癌细胞中诱导氧化应激的能力实现的,这通过丙二醛(MDA)和谷胱甘肽(GSH)水平的升高表明。因此,活性氧(ROS)调控可能是香豆素类化合物用于癌症治疗的潜在靶点,因为与正常细胞相比,癌细胞具有改变的氧化还原平衡。根据ADMET分析,所研究的化合物显示出与维生素C和没食子酸相似的良好药代动力学和毒理学特征,这使其成为在工业和医学各个领域应用的良好候选物。