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1)  oxazolidinone antibacterial
噁唑烷酮类抗菌药物
2)  oxazolidinone derivatives
噁唑烷酮类化合物
1.
Modification of novel oxazolidinone derivatives at C-5 side chain and their antibacterial activities;
新型噁唑烷酮类化合物5-位侧链的结构改造及抗菌活性
3)  oxazolindinone derivatives
噁唑烷酮衍生物
1.
Synthesis and antibacterial activity of(S)-5-acetylaminomethyl-3-[(4-substituted-aminomethyl)phenyl]-2-oxazolindinone derivatives;
(S)-5-乙酰胺甲基-3-[(4-取代胺甲基)苯基]-2-噁唑烷酮衍生物的合成及抗菌活性
4)  oxazolidinones
噁唑烷酮
1.
Synthesis and Antibacterial Activity of(S)-5-Acetamidomethyl-3-[(3-chloro-4-substituted aminomethyl)phenyl]-2-oxazolidinones;
(S)-5-乙酰胺甲基-3-[(3-氯-4-取代胺甲基)苯基]-2-噁唑烷酮的合成及抗菌活性
2.
Linezolid is a new class of oxazolidinones antibacterial agents that has been first used in clinical,it inhibits bacterial protein synthesis by blocking the formation of initiation complex.
利奈唑胺(linezolid)是第一个应用于临床的新型噁唑烷酮类抗生素,通过抑制蛋白起始复合物的形成抑制细菌蛋白质合成,在体内、外对葡萄球菌、链球菌、肠球菌等耐药G+菌有广谱的抗菌作用,其临床疗效已经得到一系列Ⅲ期临床研究证明。
3.
The oxazolidinones are a new class of totally synthetic antibacterials that inhibit protein synthesis via binding to a distinct region of 23S RNA of the 50S ribosomal subunit in prokaryotes.
噁唑烷酮类抗菌剂是一类新型的全合成抗菌药物,作用于细菌蛋白质合成的早期阶段(主要作用靶点是核糖体50S亚基的23S rRNA),表现出高度的抗耐药性革兰氏阳性菌活性,其代表药物吗啉噁酮(linezolid)已上市。
5)  oxazolidinone
噁唑烷酮
1.
Analysis of (4S)-4-benzyl-3-(2′(E)-butenyl)-2-oxazolidinone by nuclear magnetic resonance;
(4S)-4-苄基-3-(2’(E)-丁烯酰基)-2-噁唑烷酮的核磁分析
2.
Studies on synthesis of NCPS supported oxazolidinone chiral auxiliary;
线型聚苯乙烯支载噁唑烷酮手性助剂的合成研究
3.
Preparation of (S)-(+)-4-Phenyl-2-oxazolidinone;
手性4-苯基-2-噁唑烷酮的合成研究
6)  famoxadone
噁唑菌酮
1.
Study on residue dynamics of famoxadone in citrus;
噁唑菌酮在柑橘上的残留动态研究
2.
A simple and rapid method had been established, which determines the residue amount of famoxadone in soil by RP-HPLC with the phenyl column as chromatographic column.
01mol/L的磷酸二氢钾(体积比45∶55,pH=3)为流动相,测定土壤中易保有效成分噁唑菌酮残留量的反相高效液相色谱分析方法。
补充资料:噁唑
分子式:暂无
分子量:暂无
CAS号:288-42-6

性质:暂无

制备方法:暂无

用途:暂无

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