Department of Chemistry, Biology and Biotechnology, Bialystok University of Technology, Wiejska 45E Street, 15-351 Bialystok, Poland.
Institute of Nuclear Chemistry and Technology, 16 Dorodna Street, 03-195 Warsaw, Poland.
Nutrients. 2021 Sep 4;13(9):3107. doi: 10.3390/nu13093107.
Seven derivatives of plant-derived hydroxybenzoic acid (HBA)-including 2,3-dihydroxybenzoic (2,3-DHB, pyrocatechuic), 2,4-dihydroxybenzoic (2,4-DHB, β-resorcylic), 2,5-dihydroxybenzoic (2,5-DHB, gentisic), 2,6-dihydroxybenzoic (2,6-DHB, γ-resorcylic acid), 3,4-dihydroxybenzoic (3,4-DHB, protocatechuic), 3,5-dihydroxybenzoic (3,5-DHB, α-resorcylic), and 3,4,5-trihydroxybenzoic (3,4,5-THB, gallic) acids-were studied for their structural and biological properties. Anti-/pro-oxidant properties were evaluated by using DPPH (2,2-diphenyl-1-picrylhydrazyl), ABTS (2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), FRAP (ferric-reducing antioxidant power), CUPRAC (cupric-reducing antioxidant power), and Trolox oxidation assays. Lipophilicity was estimated by means of experimental (HPLC) and theoretical methods. The antimicrobial activity against (), (), (), (), (), and () was studied. The cytotoxicity of HBAs in MCF-7 and MDA-MB-231 cell lines was estimated. Moreover, the structure of HBAs was studied by means of experimental (FTIR, H, and C NMR) and quantum chemical DFT methods (the NBO and CHelpG charges, electrostatic potential maps, and electronic parameters based on the energy of HOMO and LUMO orbitals). The aromaticity of HBA was studied based on the calculated geometric and magnetic aromaticity indices (HOMA, Aj, BAC, I6, NICS). The biological activity of hydroxybenzoic acids was discussed in relation to their geometry, the electronic charge distribution in their molecules, their lipophilicity, and their acidity. Principal component analysis (PCA) was used in the statistical analysis of the obtained data and the discussion of the dependency between the structure and activity (SAR: structure-activity relationship) of HBAs. This work provides valuable information on the potential application of hydroxybenzoic acids as bioactive components in dietary supplements, functional foods, or even drugs.
七种植物源羟基苯甲酸(HBA)衍生物,包括 2,3-二羟基苯甲酸(2,3-DHB,焦儿茶酸)、2,4-二羟基苯甲酸(2,4-DHB,β-间苯二酚)、2,5-二羟基苯甲酸(2,5-DHB,龙胆酸)、2,6-二羟基苯甲酸(2,6-DHB,γ-间苯二酚酸)、3,4-二羟基苯甲酸(3,4-DHB,原儿茶酸)、3,5-二羟基苯甲酸(3,5-DHB,α-间苯二酚)和 3,4,5-三羟基苯甲酸(3,4,5-THB,没食子酸),都对其结构和生物性质进行了研究。通过 DPPH(2,2-二苯基-1-苦基肼基)、ABTS(2,2-偶氮-双(3-乙基苯并噻唑啉-6-磺酸))、FRAP(铁还原抗氧化能力)、CUPRAC(铜还原抗氧化能力)和 Trolox 氧化测定法来评估抗/抗氧化性能。通过实验(HPLC)和理论方法来估算亲脂性。研究了对 ()、 ()、 ()、 ()、 ()和 ()的抑菌活性。在 MCF-7 和 MDA-MB-231 细胞系中评估了 HBAs 的细胞毒性。此外,通过实验(FTIR、H 和 C NMR)和量子化学 DFT 方法(NBO 和 CHelpG 电荷、静电势能图和基于 HOMO 和 LUMO 轨道能量的电子参数)研究了 HBAs 的结构。基于计算的几何和磁芳香性指数(HOMA、Aj、BAC、I6、NICS)研究了 HBA 的芳香性。根据羟基苯甲酸的几何形状、分子中电子电荷分布、亲脂性和酸度讨论了羟基苯甲酸的生物活性。主成分分析(PCA)用于对获得的数据进行统计分析,并讨论 HBAs 的结构与活性(SAR:结构-活性关系)之间的关系。这项工作为羟基苯甲酸作为膳食补充剂、功能性食品甚至药物中的生物活性成分的潜在应用提供了有价值的信息。