Effect of 4-methoxy 1-methyl 2-oxopyridine 3-carbamide on Staphylococcus aureus by inhibiting UDP-MurNAc-pentapeptide, peptidyl deformylase and uridine monophosphate kinase

首页> 外文期刊>Journal of applied microbiology >Effect of 4-methoxy 1-methyl 2-oxopyridine 3-carbamide on Staphylococcus aureus by inhibiting UDP-MurNAc-pentapeptide, peptidyl deformylase and uridine monophosphate kinase

【24h】

Effect of 4-methoxy 1-methyl 2-oxopyridine 3-carbamide on Staphylococcus aureus by inhibiting UDP-MurNAc-pentapeptide, peptidyl deformylase and uridine monophosphate kinase

机译：通过抑制UDP-Murnac-五肽，肽基杂化酶和尿苷一磷酸氨基磷酶，4-甲氧基1-甲基2-氧吡啶3-氨基甲酰胺对金黄色葡萄球菌的影响

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Aims The present study aimed to investigate the anti-Staphylococcus aureus and anti-biofilm properties of 4-methoxy-1-methyl-2-oxopyridine-3-carbamide (MMOXC) on S. aureus UDP-MurNAc-pentapeptide (MurF), peptidyl deformylase (PDF) and uridine monophosphate kinase (UMPK).

机译：目前的研究旨在探讨4-甲氧基-1-甲基-2-氧吡啶-3-氨基甲酰胺（MMOXC）的抗葡萄球菌和抗生物膜性质在S.UUREUS UDP-MURNAC-五肽（MURF），肽基脱晶体（PDF）和尿苷一磷酸激酶（UMPK）。

著录项

来源
《Journal of applied microbiology》 |2017年第3期|共13页
作者

展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类应用微生物学;
关键词
anti-biofilm; IC; (50); K-i; MIC; PCR; real-time ZOI;

机译：抗生物膜;IC;（50）;K-I;麦克风;PCR;实时ZOI;

相似文献

外文文献
中文文献
专利

1. Effect of 4-methoxy 1-methyl 2-oxopyridine 3-carbamide on Staphylococcus aureus by inhibiting UDP-MurNAc-pentapeptide, peptidyl deformylase and uridine monophosphate kinase [J] . Journal of applied microbiology . 2017,第3期

机译：通过抑制UDP-Murnac-五肽，肽基杂化酶和尿苷一磷酸氨基磷酶，4-甲氧基1-甲基2-氧吡啶3-氨基甲酰胺对金黄色葡萄球菌的影响
2. Cellular Pharmacokinetics and Intracellular Activity of the Novel Peptide Deformylase Inhibitor GSK1322322 against Staphylococcus aureus Laboratory and Clinical Strains with Various Resistance Phenotypes: Studies with Human THP-1 Monocytes and J774 Murine Macrophages [J] . Peyrusson Frederic, Butler Deborah, Tulkens Paul M., Antimicrobial agents and chemotherapy. . 2015,第9期

机译：新型肽脱甲酰基酶抑制剂GSK1322322对金黄色葡萄球菌实验室和具有不同抗性表型的临床菌株的细胞药代动力学和细胞内活性：人类THP-1单核细胞和J774小鼠巨噬细胞的研究。
3. Frequency of Spontaneous Resistance to Peptide Deformylase Inhibitor GSK1322322 in Haemophilus influenzae, Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus pneumoniae [J] . Min Sharon, Ingraham Karen, Huang Jianzhong, Antimicrobial agents and chemotherapy. . 2015,第8期

机译：流感嗜血杆菌，金黄色葡萄球菌，化脓性链球菌和肺炎链球菌对肽脱甲酰酶抑制剂GSK1322322的自发抵抗频率
4. Inhibiting Staphylococcus aureus antibiotic resistance via photodisassembly of membrane microdomains [C] . Jie Hui, Pu-Ting Dong, Lijia Liang, Society of Photo-Optical Instrumentation Engineers;Conference on Photonic Diagnosis, Monitoring, Prevention, and Treatment of Infections and Inflammatory Diseases . 2020

机译：通过光解膜微区抑制金黄色葡萄球菌抗生素抗性
5. Copper Dependent Inhibitors Subvert Common Resistance Mechanisms in Staphylococcus aureus and Inhibit Crucial Metabolic Pathways [D] . Crawford, Cameron Lee. 2020

机译：铜依赖性抑制剂在金黄色葡萄球菌中颠覆公共抗性机制，抑制至关重要的代谢途径
6. Iron enhances the peptidyl deformylase activity and biofilm formation in Staphylococcus aureus [O] . Vimjam Swarupa, Abhijit Chaudhury, Potukuchi Venkata Gurunadha Krishna Sarma 2018

机译：铁增强金黄色葡萄球菌中的肽基去甲酰基酶活性和生物膜形成
7. Structure of Staphylococcus aureus cytidine monophosphate kinase in complex with cytidine 5'-monophosphate. [O] . Dhaliwal, B, Ren, J, Lockyer, M, 2006

机译：金黄色葡萄球菌胞苷单磷酸激酶与胞苷5'-单磷酸复合的结构。

Effect of 4-methoxy 1-methyl 2-oxopyridine 3-carbamide on Staphylococcus aureus by inhibiting UDP-MurNAc-pentapeptide, peptidyl deformylase and uridine monophosphate kinase

摘要

著录项

相似文献

相关主题

期刊订阅