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Vebufloxacin (Flumenique) Sale

(Synonyms: 维布沙星,Flumenique; OPC7241; DM8966) 目录号 : GC33708

Vebufloxacin (Flumenique) (Flumenique; OPC7241; DM8966) 对革兰氏阳性和阴性细菌具有有效的抗菌活性。

Vebufloxacin (Flumenique) Chemical Structure

Cas No.:79644-90-9

规格 价格 库存 购买数量
1mg
¥5,177.00
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5mg
¥10,264.00
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10mg
¥17,493.00
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20mg
¥30,791.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Vebufloxacin (Flumenique; OPC7241; DM8966) exhibits potent antibacterial activity against gram-positive and -negative bacteria.

A series of substituted 6,7-dihydro-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carboxylic acids is synthesized and tested for antibacterial activities. Among them, Vebufloxacin (OPC-7241) exhibits potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and Pseudomonas aeruginosa, and OPC-7251 shows potent activity characteristically against Propionibacterium acnes[1].

[1]. Ishikawa H, et al. Studies on antibacterial agents. I. Synthesis of substituted 6,7-dihydro-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carboxylic acids. Chem Pharm Bull (Tokyo). 1989 Aug;37(8):2103-8.

Chemical Properties

Cas No. 79644-90-9 SDF
别名 维布沙星,Flumenique; OPC7241; DM8966
Canonical SMILES O=C(C1=CN2C(C)CCC3=C2C(C1=O)=CC(F)=C3N4CCN(C)CC4)O
分子式 C19H22FN3O3 分子量 359.39
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 2.7825 mL 13.9125 mL 27.8249 mL
5 mM 0.5565 mL 2.7825 mL 5.565 mL
10 mM 0.2782 mL 1.3912 mL 2.7825 mL
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Research Update

Dispersive liquid-liquid microextraction of quinolones in porcine blood: Validation of a CE method using univariate calibration or multivariate curve resolution-alternating least squares for overlapped peaks

Electrophoresis 2017 Apr;38(8):1122-1129.PMID:28177131DOI:10.1002/elps.201600475

In the previously published part of this study, we detailed a novel strategy based on dispersive liquid-liquid microextraction to extract and preconcentrate nine fluoroquinolones in porcine blood. Moreover, we presented the optimized experimental conditions to obtain complete CE separation between target analytes. Consequently, this second part reports the validation of the developed method to determine Flumenique, difloxacin, enrofloxacin, marbofloxacin, ofloxacin, ciprofloxacin, through univariate calibration, and enoxacin, danofloxacin, and gatifloxacin through multivariate curve resolution analysis. The validation was performed according to FDA guidelines for bioanalytical assay procedures and the European Directive 2002/657 to demonstrate that the results are reliable. The method was applied for the determination of fluoroquinolones in real samples. Results indicated a high selectivity and excellent precision characteristics, with RSD less than 11.9% in the concentrations, in intra- and interassay precision studies. Linearity was proved for a range from 4.00 to 30.00 mg/L and the recovery has been investigated at four different fortification levels, from 89 to 113%. Several approaches found in the literature were used to determinate the LODs and LOQs. Though all strategies used were appropriate, we obtained different values when using different methods. Estimating the S/N ratio with the mean noise level in the migration time of each fluoroquinolones turned out as the best studied method for evaluating the LODs and LOQs, and the values were in a range of 1.55 to 4.55 mg/L and 5.17 to 9.62 mg/L, respectively.