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Ciprofloxacin

Ciprofloxacin

产品编号 T1640   CAS 85721-33-1
别名: Ciproxan, 环丙沙星, Ciprobay, Bay o 9867, Bay-09867

Ciprofloxacin (Bay-09867) 是一种有高抗菌活性的氟喹诺酮类抗生素。

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Ciprofloxacin Chemical Structure
Ciprofloxacin, CAS 85721-33-1
规格 价格/CNY 货期 数量
500 mg ¥ 225 现货
1 g ¥ 333 现货
5 g ¥ 671 现货
1 mL (in DMSO) ¥ 195 现货
产品目录号及名称: Ciprofloxacin (T1640)
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纯度: 99.89%
纯度: 99.65%
纯度: 98.77%
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生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 Ciprofloxacin (Bay-09867), a synthetic broad spectrum fluoroquinolone antibiotic, inhibits bacterial DNA gyrase. It is more active against Gram-negative bacteria than Gram-positive bacteria.
体内活性 Ciprofloxacin (1 mg/L) induces GST activity, in contrast with inhibited GST and CAT of larvae exposed to enrofloxacin. Ciprofloxacin (≥10 μg/L) and enrofloxacin are ecotoxic for development, growth, detoxifying, and oxidative stress enzymes in anuran amphibian larvae[4]. Ciprofloxacin (CIP) shows potent activity against Y. pestis with MIC90 of 0.03 μg/mL[2]. In a murine model of pneumonic plague, ciprofloxacin (30 mg/kg, i.p.) results in a drug exposure which is similar to the drug exposure observed in humans following a 500 mg dose of oral ciprofloxacin. Intraperitoneal ciprofloxacin reduces the lung bacterial load compared to controls treated with intraperitoneal PBS[5].
激酶实验 The in vitro kinase assays is performed by incubating purified kinase (IKKε or TBK1) in kinase buffer containing 25 mM Tris (pH7.5), 10 mM MgCl2, 1 mM DTT, and 10 μM ATP for 30 minutes at 30°C in the presence of 0.5 μCi γ-[32P]-ATP and 1 μg MBP per sample as a substrate. The kinase reaction is stopped by adding 4x sodium dodecyl sulfate (SDS) sample buffer and boiling for 5 minutes at 95°C. Supernatants are resolved by SDS-polyacrylamide gel electrophoresis, transferred to nitrocellulose, and analyzed by autoradiography using a Typhoon 9410 phosphorimager.
别名 Ciproxan, 环丙沙星, Ciprobay, Bay o 9867, Bay-09867
分子量 331.34
分子式 C17H18FN3O3
CAS No. 85721-33-1

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

H2O: Insoluble

DMSO: 0.33 mg/mL (1 mM), Sonication is recommended.

0.1 M HCl: 2 mg/mL (6.04 mM), Sonication is recommended.

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO / 0.1 M HCl 1 mM 3.018 mL 15.0902 mL 30.1805 mL 75.4512 mL
0.1 M HCl 5 mM 0.6036 mL 3.018 mL 6.0361 mL 15.0902 mL

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TargetMol Library Books参考文献

1. Wise R, et al. Antimicrob Agents Chemother, 1983, 23(4), 559-564. 2. Pan XS, et al. Antimicrob Agents Chemother, 1996, 40(10), 2321-2326. 3. Lacy MK, et al. Antimicrob Agents Chemother, 1999, 43(3), 672-677. 4. Peltzer PM, et al. Ecotoxicity of veterinary enrofloxacin and ciprofloxacin antibiotics on anuran amphibian larvae. Environ Toxicol Pharmacol. 2017 Feb 4. pii: S1382-6689(17)320029-7. 5. Hamblin KA, et al. Inhaled Liposomal Ciprofloxacin Protects against a Lethal Infection in a Murine Model of Pneumonic Plague. Front Microbiol. 2017 Feb 6;8:91. 6. Steenbergen J, et al. In Vitro and In Vivo Activity of Omadacycline Against Two Biothreat Pathogens: Bacillus anthracis and Yersinia pestis. Antimicrob Agents Chemother. 2017 Feb 21.
Topoisomerase IV inhibitor 1 Topoisomerase IV inhibitor 2 Ellipticine Topoisomerase I inhibitor 9 NU2058 Topoisomerase I inhibitor 10 Aurintricarboxylic acid Groenlandicine

相关化合物库

该产品包含在如下化合物库中:
药物功能重定位化合物库 上市药物库 抗菌活性库 经典已知活性库 抑制剂库 已知活性化合物库 口服活性化合物库 抗生素库 FDA上市及药典收录分子库 临床期小分子药物库

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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: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。

母液配置方法:2 mg 药物溶于 50 μL DMSO (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:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

Ciprofloxacin 85721-33-1 DNA Damage/DNA Repair Microbiology/Virology Topoisomerase Antibacterial Antibiotic Bay 09867 Bacterial Apoptosis Reactive Oxygen Species anti-proliferative Inhibitor mitochondrial inhibit ROS Bay09867 Ciproxan Mitochondrial Metabolism 环丙沙星 DNA damage DNA Ciprobay Bay o 9867 Bay-09867 inhibitor

 

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