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Rufloxacin hydrochloride

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纯度: 99.80%

货号 TQ0221Cas号 106017-08-7

别名 盐酸芦氟沙星, MF-934 hydrochloride

Rufloxacin hydrochloride (MF-934 hydrochloride) 是一种氟喹诺酮类抗菌剂,可抑制拓扑异构酶。 Rufloxacin hydrochloride 抑制人单核细胞中的 B 细胞分化。

Rufloxacin hydrochloride
其他形式的 “Rufloxacin hydrochloride”:

Rufloxacin hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.80%

货号 TQ0221 别名 盐酸芦氟沙星, MF-934 hydrochlorideCas号 106017-08-7

Rufloxacin hydrochloride (MF-934 hydrochloride) 是一种氟喹诺酮类抗菌剂,可抑制拓扑异构酶。 Rufloxacin hydrochloride 抑制人单核细胞中的 B 细胞分化。

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25 mg
¥ 295
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50 mg
¥ 417
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100 mg
¥ 671
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产品介绍


生物活性
产品描述
Rufloxacin hydrochloride (MF-934 hydrochloride) is a fluoroquinolone antibacterial and inhibits topoisomerase. Rufloxacin hydrochloride inhibits B-cell differentiation in human mononuclear cells.
别名盐酸芦氟沙星, MF-934 hydrochloride
化学信息
分子量399.867
分子式C17H19ClFN3O3S
CAS No.106017-08-7
SmilesCl.CN1CCN(CC1)c1c(F)cc2c3c1SCCn3cc(C(O)=O)c2=O
密度no data available
颜色White
物理性状Solid
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
H2O: 1 mg/mL (2.5 mM), Sonication is recommended.
DMSO: 0.08 mg/mL (0.2 mM), Sonication and heating are recommended.

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

TargetMol AI Summary
Rufloxacin hydrochloride shows bioactivity across a spectrum of biological assays targeting various enzymes and pathogens. It exhibits nanomolar potency in inhibiting enzymes such as HSD17B4, JMJD2E, ALDH1A1, HPGD, HADH2, and the histone lysine methyltransferase G9a. The compound also demonstrates inhibitory activity against non-replicating, drug-tolerant Mycobacterium tuberculosis, the malarial parasite plastid, and specific regions in Salmonella Typhimurium and Salmonella typhi. Furthermore, Rufloxacin hydrochloride inhibits cellular entry mechanisms of the Ebola virus. In terms of antiviral activity, Rufloxacin hydrochloride shows efficacy against SARS-CoV-2 by inhibiting cytotoxicity in Caco-2 cells and VERO-6 cells at a concentration of 10 µM, with reported inhibition rates of 17.62% and 0.01% respectively after 48 hours. It also inhibits the SARS-CoV-2 3CL-Pro protease with an inhibition rate of 12.56% at a 20 µM concentration. Additionally, Rufloxacin hydrochloride displays antifungal activity against Candida albicans and Cryptococcus neoformans with MIC values greater than 10,000 nM. Its antibacterial activity spans various bacteria, including Escherichia coli (MIC 1,250 nM), Pseudomonas aeruginosa (MIC 10,000 nM), Staphylococcus aureus MRSA (MIC 2,500 nM), Klebsiella pneumoniae, and Acinetobacter baumannii (both with MIC values greater than 10,000 nM). It has a cytotoxicity (CC50) greater than 10,000 nM against HEK293 cells. Overall, Rufloxacin hydrochloride exhibits a broad range of bioactivities against enzymes, pathogens, and viruses..
Note: Summary generated by AI, AI may be wrong some times, we do not provide any medical advice and only sell our product to accredited institution, Please cross-check with other sources, data source: chembl
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