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Synthesis and evaluation of antibacterial activities of andrographolide analogues.

机译:穿心莲内酯类似物的合成和抗菌活性评估。

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Andrographolide (Andro), the main active component of the herb Andrographis paniculata, has been used for many years to treat a variety of diseases including bacterial and viral infections. Andro was recently reported to act by inhibiting the bacterial quorum sensing system. We have synthesized several Andro analogues and investigated their antibacterial activity and mechanism of action. The new compounds were found to be much more potent than the parent Andro in inhibiting bacterial growth and quorum sensing system. Compounds 5 and 7 significantly reduced virulence factor production. Compound 7 completely inhibited Pseudomonas aeruginosa (P. aeruginosa) biofilm formation, and exhibited synergistic activity with conventional antibiotics. These findings suggest that compound 7 may be the basis for future drug development to combat the unmet needs of virulence factor production, biofilm formation and antibiotic resistance.
机译:穿心莲内酯(Andro)是穿心莲药材的主要活性成分,已被用于治疗多种疾病,包括细菌和病毒感染。最近有报道说安德罗通过抑制细菌群体感应系统起作用。我们已经合成了几种Andro类似物,并研究了它们的抗菌活性和作用机理。发现新化合物在抑制细菌生长和群体感应系统方面比母体安德罗(Andro)更有效。化合物5和7显着降低了毒力因子的产生。化合物7完全抑制铜绿假单胞菌(P. aeruginosa)生物膜形成,并表现出与常规抗生素的协同活性。这些发现表明,化合物7可能是未来药物开发的基础,以解决毒力因子生产,生物膜形成和抗生素抗性的未满足需求。

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