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84294-96-2

中文名称 依诺沙星
英文名称 Enoxacin
CAS 84294-96-2
分子式 C15H17FN4O3.11/2H2O
分子量 694.684
MOL 文件 84294-96-2.mol
更新日期 2024/04/28 11:50:47
84294-96-2 结构式 84294-96-2 结构式

基本信息

中文别名
依诺沙星倍
水合依诺沙星
依诺沙星水合物
依诺沙星半水合物
依诺沙星倍半水合物
依诺沙星(1.5结晶水合物)
依诺沙星(1.5结晶水合物) 标准品
1-乙基-6-氟-4-氧代-7-(哌嗪-1-基)-1,4-二氢-1,8-萘啶-3-羧酸倍半水合物
英文别名
Enoxacin sesq
CI-919 hydrate
AT-2266 hydrate
Enoxacin (hydrate)
ENOXACIN SESQUIHYDRATE
EnoxacinSesquihydrate>
Enoxacin hydrate (CI-919)
1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic acid sesquihydrate
bis(1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-di hydro-1,8-naphthyridine-3-carboxylic acid) trihydrate C30H

物理化学性质

熔点226 °C
储存条件Keep in dark place,Inert atmosphere,Room temperature
溶解度可溶于MNaOH:溶解度为50mg/mL,澄清,无色至淡黄色
形态neat
Merck14,3587

安全数据

安全说明24/25
WGK Germany3
海关编码29335990
依诺沙星价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/01/25HY-B0268A依诺沙星
Enoxacin hydrate
84294-96-2100mg500元
2024/01/25HY-B0268A依诺沙星
Enoxacin hydrate
84294-96-2500mg800元
2024/01/16E0762依诺沙星倍半水合物
Enoxacin  Sesquihydrate
84294-96-25G370元

常见问题列表

生物活性
Enoxacin sesquihydrate (Enoxacin hydrate)是一种广谱的6-fluoronaphthyridinone抗菌剂。
体外研究

Enoxacin hydrate (Enoxacin sesquihydrate) increases siGFP-mediated gene knockdown mediated by siRNA against EGFP in HEK293 cells-based reporter system in a dose-dependent manner, with a median effective concentration (EC50) of ~30 µM, whereas it has no effect on the cells expressing GFP only. Enoxacin (50 µM) promotes the processing of miRNAs and the loading of siRNA duplexes onto RISCs in HEK293 cells.
Enoxacin has no effect on the processing of pre-let-7 or pre-miR-30a by Dicer alone. However, the addition of Enoxacin can enhance the processing of let-7 or pre-miR-30a by Dicer and TRBP together.
Enoxacin inhibits 90% Escherichia coli, Klebsiella sp., Aeromonas sp., Enterobacter spp., Serratia spp., Proteus mirabilis, and Morganella morganii at less than or equal to 0.8 micrograms/ml.

体内研究

Enoxacin hydrate (Enoxacin sesquihydrate; 100 µM; 2 µl; injected into ear once a day for 3 consecutive days (days 12, 13 and 14)) enhances the the GFP mRNA knockdown efficiency by Lv-siGFP (from 80% to 60%; 40% GFP mRNA level remained), whereas alone has no effect on GFP expression in GFP transgenic line C57BL/6-Tg(ACTB-EGFP)1Osb/J (10 d old) with lentivirus expressing shGFP (Lv-siGFP; injected into ear for 10 days).

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