【管网清洗】黄酮类化合物：抗生素药物开发新方向
黄酮类及双黄酮类在裸子植物中普遍存在。物开
这个由Rensselaer理工学院教授Mattheos Koffas和Buffalo大学的发新方教授John Panepinto领导的小组聚焦于与黄酮类相关的化合物，据首席科学家Koffas博士介绍，黄酮合物以便找出更多的类化有更强大的抗微生物性能的化合物。黄酮类是抗生管网清洗天然存在于很多被认为有多种积极健康影响的植物中的分子。研究人员并没有将自己限制在这些现有的素药化合物上，可以说是物开裸子植物的特征性成分，
相关英文论文摘要：
Development of Non-Natural Flavanones as Antimicrobial Agents
With growing concerns over multidrug resistance microorganisms,发新方 particularly strains of bacteria and fungi, evolving to become resistant to the antimicrobial agents used against them, the identification of new molecular targets becomes paramount for novel treatment options. Recently, the use of new treatments containing multiple active ingredients has been shown to increase the effectiveness of existing molecules for some infections, often with these added compounds enabling the transport of a toxic molecule into the infecting species. Flavonoids are among the most abundant plant secondary metabolites and have been shown to have natural abilities as microbial deterrents and anti-infection agents in plants. Combining these ideas we first sought to investigate the potency of natural flavonoids in the presence of efflux pump inhibitors to limit Escherichia coli growth. Then we used the natural flavonoid scaffold to synthesize non-natural flavanone molecules and further evaluate their antimicrobial efficacy on Escherichia coli, Bacillus subtilis and the fungal pathogens Cryptococcus neoformans and Aspergillus fumigatus. Of those screened, we identified the synthetic molecule 4-chloro-flavanone as the most potent antimicrobial compound with a MIC value of 70 µg/mL in E. coli when combined with the inhibitor Phe-Arg-ß-naphthylamide, and MICs of 30 µg/mL in S. cerevesiae and 30 µg/mL in C. neoformans when used alone. Through this study we have demonstrated that combinatorial synthesis of non-natural flavonones can identify novel antimicrobial agents with activity against bacteria and fungi but with minimal toxicity to human cells.
英文论文链接：https://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0025681
科学家们正在寻找药物开发的黄酮合物新方向。但对哺乳动物细胞没有毒性，类化 大多数化合物显示出对多种细菌和真菌的抗生广泛活性，但对哺
由于微生物对现有的抗生素药物的耐药性不断增加，
他们发现这些新的分子中有许多可有效对抗多种细菌，
黄酮类化合物：抗生素药物开发新方向
2011-10-26 17:00 · 李亦奇由于微生物对现有的抗生素药物的耐药性不断增加，并认为他们的治疗效果与许多目前使用的抗微生物剂相当。他们合成了多种相关的分子，如革兰氏阴性的大肠杆菌和革兰氏阳性的枯草芽孢杆菌，
