Dual-action gallium-flavonoid compounds for combating Pseudomonas aeruginosa infection
文献信息
Bingjie Han, Yu Guo, Richard Y T Kao, Hongyan Li, Hongzhe Sun, Wei Xia
The opportunistic pathogen Pseudomonas aeruginosa (P. aeruginosa) causes infections that are difficult to treat, which is due to the bacterial natural resistance to antibiotics. The bacterium is also able to form a biofilm that protects the bacterium from clearance by the human immune system and leads to chronic infection. Herein, we synthesized and characterized a novel gallium compound that interferes with both the iron metabolism and quorum sensing system of P. aeruginosa to achieve a significant bactericidal activity. The compound could substantially reduce the secretion of bacterial virulence factors as well as eliminate biofilm formation. Integrative omics analysis indicates that this compound can significantly disturb the gene transcription and metabolism of P. aeruginosa. The effectiveness of the gallium compound was further validated in mammalian cell and murine skin infection models. Our study offers a new strategy to design new gallium-based antimicrobials to combat P. aeruginosa infection.
相关文献
Coupled stochastic simulation of the chain length and particle size distribution in miniemulsion radical copolymerization of styrene and N-vinylcaprolactam
Paul H. M. Van Steenberge
DOI: 10.1039/C9RE00218A
NH3-SCR of NO with novel active, supported vanadium-containing Keggin-type heteropolyacid catalysts
Anna Bukowski, Leonhard Schill, David Nielsen, Susanne Mossin, Anders Riisager, Jakob Albert
DOI: 10.1039/D0RE00033G
Synthesis of hybrid semiconducting polymer–metal latexes
Christine Labrugère
DOI: 10.1039/C2PY20602A
Reducing polyazomethine to poly(N-phenylbenzylamine) with near infrared electrochromic, fluorescence and photovoltaic properties
Jiwei Cai, Ping Zhao, Haijun Niu, Yongfu Lian, Cheng Wang, Xuduo Bai, Wen Wang
DOI: 10.1039/C2PY20846F
Exploring shape amphiphiles beyond giant surfactants: molecular design and click synthesis
Kan Yue, Chang Liu, Kai Guo, Kan Wu, Xue-Hui Dong, Hao Liu, Mingjun Huang, Stephen Z. D. Cheng, Wen-Bin Zhang
DOI: 10.1039/C2PY20881D
New insights into catalysis for Heck reactions with fine supported Pd particles
Lin Huang, Zhan Wang, Jozel Tan
DOI: 10.1039/C9RE00480G
Thiophene spacers impart crystallinity and enhance the efficiency of benzotrithiophene-based conjugated polymers for bulk heterojunction photovoltaics
Shang-Che Lan, Po-An Yang, Meng-Jie Zhu, Chia-Min Yu, Jian-Ming Jiang, Kung-Hwa Wei
DOI: 10.1039/C2PY20819A
Kinetic study of esterification over structured ZSM-5-coated catalysts based on fluid flow situations in macrocellular foam materials
Xin Gao, Qiuyan Ding, Yan Wu, Yilai Jiao, Jinsong Zhang, Xingang Li, Hong Li
DOI: 10.1039/C9RE00445A
Identification of strategic molecules for future circular supply chains using large reaction networks
Jana Marie Weber, Pietro Lió
DOI: 10.1039/C9RE00213H
您可能还喜欢
4-[4-三氟甲基苯基]恶唑(CAS号:1126636-40-5)通常如何合成?
4-[4-三氟甲基苯基]恶唑通常通过将4-三氟甲基苯酚与异硫氰酸苯酯在有机溶剂中进行酯化反应合成。该反应可在无水条件下,使用适当的催化剂,如四丁基氢氧化铵,以提...
RockPhos Pd G3(CAS号:2009020-38-4)通常如何合成?
RockPhos Pd G3 通常通过钯催化偶联反应合成,使用配体 (2'-Amino-2-biphenylyl)(methanesulfonato-kappa...
1-哌啶甲酰胺(CAS号:2158-03-4)的市场或研究趋势如何?
1-哌啶甲酰胺作为有机合成中的重要中间体,其市场需求主要受医药、农药、染料等行业推动。近年来,随着新药开发和绿色化学的发展,该化合物的研究趋势集中在开发更高效、...
2-(二苯基膦基)乙胺(CAS号:4848-43-5)适用哪些法规指南?
2-(二苯基膦基)乙胺适用于多种法规指南,包括但不限于《全球化学品统一分类和标签制度》(GHS),欧盟《化学品注册、评估、授权和限制》法规(REACH),以及美...
如何储存间苯二甲酸二烯丙酯(CAS号:1087-21-4)?
间苯二甲酸二烯丙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。储存容器应密封,避免光照和高温。储存温度应控制在25℃以下,相对湿度应低于80%。避免与其...
什么是间甲苯异硫代异氰酸酯(CAS号:621-30-7)?
间甲苯异硫代异氰酸酯是一种有机化合物,分子式为C7H7NO2S,具有刺激性气味。它是一种重要的有机合成中间体,在合成其他化合物时广泛应用。
在合成中是否有N-Boc-D-苯丙氨醇(CAS号:106454-69-7)的替代品?
在合成中,可以考虑使用N-Cbz-D-苯丙氨醇或N-Fmoc-D-苯丙氨醇作为替代品。这些化合物同样具有保护氨基的功能,且在合成过程中表现出良好的反应性能。
3-羟甲基-2-氧异丙基吡啶(CAS号:954240-50-7)的主要用途是什么?
3-羟甲基-2-氧异丙基吡啶主要用于有机合成领域,可以作为合成其他药物、农药或精细化学品的中间体。此外,它还可能在实验室研究中作为特定反应的前体或溶剂。
6-氨基-9-甲基嘌呤(CAS号:700-00-5)应用于哪些行业?
6-氨基-9-甲基嘌呤目前主要应用于医药行业,作为某些药物的中间体。此外,它还可能用于聚合物、传感器和半导体的某些领域,作为功能性单体或掺杂剂。














![2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1) structure 2-{3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl}[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one hydrochloride (1:1) structure](https://cnstatic.chemtradehub.com/structs/253/25332-39-2-496e.webp)
