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Novel targets to develop new antibacterial agents and novel alternatives to antibacterial agents

机译:开发新型抗菌剂的新目标和抗菌剂的新替代品

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Antibacterial agents have saved many lives and helped the growth of modern medicine over the past half century. The emergence of drug resistance, jeopardizing the effectiveness of these life-saving treatments. This clearly highlights the urgent need for new and improved antibacterial drugs with a novel target and new molecular structure agent to obviate cross-resistance. This paper reviewed the possible new ways to discover novel antibacterial agents. The most widely studied new bacterial targets for novel drug development are quorum sensor biosynthesis, bacterial virulence factor, bacteria cell division machinery, Bacterial cell wall synthesis, PDF inhibitor, isoprenoid biosynthesis, shikimate synthesis pathway, biofilm synthesis and fatty acid biosynthesis. These new discovery routes have given rise to agents that are in preclinical trials. This review also discusses the alternatives approaches that actbacteriaor any approaches that target the host. The most advanced approaches that are on clinical development are phages and other approaches that are on preclinical development are antimicrobial peptides. These alternatives ways may use as adjunctive therapies, which suggest that conventional antibacterial agents are still essential.
机译:在过去的半个世纪中,抗菌剂挽救了许多生命,并帮助了现代医学的发展。耐药性的出现,危害了这些挽救生命的治疗方法的有效性。这清楚地突出表明了迫切需要具有新型靶标和新型分子结构剂的新型抗菌药物,以消除交叉耐药性。本文综述了发现新型抗菌剂的可能新方法。研究最广泛的新药开发新细菌靶标是群体传感器生物合成,细菌毒力因子,细菌细胞分裂机制,细菌细胞壁合成,PDF抑制剂,类异戊二烯生物合成、,草酸酯合成途径,生物膜合成和脂肪酸生物合成。这些新的发现途径引起了临床前试验中的药物治疗。这篇综述还讨论了细菌替代方法或针对宿主的任何方法。临床开发中最先进的方法是噬菌体,而临床前开发中的其他方法是抗菌肽。这些替代方法可以用作辅助疗法,这表明常规的抗菌剂仍然是必不可少的。

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