Institute of Natural Medicine, University of Toyama, 2630-Sugitani, Toyama, 930-0194, Japan.
J Nat Med. 2023 Mar;77(2):298-305. doi: 10.1007/s11418-022-01672-9. Epub 2022 Dec 26.
Investigations of antibacterial activities revealed that the incorporation of longer alkyl chains to the C-6 position in resorcylic acid conferred antibacterial properties against Staphylococcus aureus and Bacillus subtilis. The resultant olivetolic acid (OA) derivatives with n-undecyl and n-tridecyl side-chains, even those lacking the hydrophobic geranyl moiety from their C-3 positions, exhibited strong antibacterial activities against B. subtilis at a MIC value of 2.5 μM. Furthermore, the study demonstrated that the n-heptyl alkyl-chain modification at C-6 of cannabigerolic acid (CBGA) effectively enhanced the activity against B. subtilis, demonstrating the importance of the alkyl side-chain in modulating the bioactivity. Overall, the findings in this study provided insight into further evaluations of the antibacterial activities, as well as other various biological activities of OA and CBGA derivatives, especially with optimized hydrophobicities at both the alkyl and prenyl side-chain positions of the core skeleton for the discovery of novel drug seeds.
抗菌活性研究表明,将更长的烷基链引入到间苯二酚的 C-6 位赋予了其对金黄色葡萄球菌和枯草芽孢杆菌的抗菌性能。所得的橄榄酸(OA)衍生物具有 n-十一烷基和 n-十三烷基侧链,即使它们在 C-3 位缺少疏水性香叶基部分,对枯草芽孢杆菌的 MIC 值也低至 2.5 μM,表现出很强的抗菌活性。此外,该研究表明,大麻萜酚酸(CBGA)C-6 位的正庚基烷基链修饰有效地增强了对枯草芽孢杆菌的活性,这表明烷基侧链在调节生物活性方面的重要性。总的来说,本研究的结果为进一步评估 OA 和 CBGA 衍生物的抗菌活性以及其他各种生物活性提供了思路,特别是在核心骨架的烷基和烯丙基侧链位置上优化疏水性,以发现新型药物种子。