Bodet Charles, Burucoa Christophe, Rouillon Steeve, Bellin Nicolas, Taddeo Vito Alessandro, Fiorito Serena, Genovese Salvatore, Epifano Francesco
Nat Prod Commun. 2014 Sep;9(9):1299-301.
In this study, we synthesized and characterized the antibacterial activity of three naturally occurring oxyprenylated chalcones {xinjiachalcone A (1), (2E)-1-{2,6-dihydroxy-4-[(3-methylbut-2-enyl)oxy]phenyl}-3-(4-hydroxyphenyl)prop-2-en-1-one (2), (2E)-1-{2,6-dihydroxy-4-[(3-methylbut-2-enyl)oxy]phenyl}-3-phenylprop-2-en-1-one (3), and lawsone 2-isopentenyl ether (4)}. Using several strains of Helicobacter pylori, including clinical ones, minimum inhibitory concentration (MIC) values and bactericidal activities of these compounds were determined. Xinjiachalcone A (1), active principle of Glycyrrhiza inflata Batalin, was the most effective compound, showing both a low MIC and a strong bactericidal activity against H. pylori. This study suggests that these compounds represent potential natural molecules for the prevention and treatment of H. pylori associated diseases.
在本研究中,我们合成并表征了三种天然存在的氧代异戊烯基查耳酮{新假查耳酮A(1)、(2E)-1-{2,6-二羟基-4-[(3-甲基丁-2-烯基)氧基]苯基}-3-(4-羟基苯基)丙-2-烯-1-酮(2)、(2E)-1-{2,6-二羟基-4-[(3-甲基丁-2-烯基)氧基]苯基}-3-苯基丙-2-烯-1-酮(3)以及 Lawson 2-异戊烯基醚(4)}的抗菌活性。使用包括临床菌株在内的几种幽门螺杆菌菌株,测定了这些化合物的最低抑菌浓度(MIC)值和杀菌活性。胀果甘草的活性成分新假查耳酮A(1)是最有效的化合物,对幽门螺杆菌显示出低MIC和强杀菌活性。本研究表明,这些化合物是预防和治疗幽门螺杆菌相关疾病的潜在天然分子。