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Besifloxacin Hydrochloride

🥰Excellent
Catalog No. T6406Cas No. 405165-61-9
Alias BOL-303224-A, Besivance hydrochloride, Besifloxacin HCl

Besifloxacin Hydrochloride (BOL-303224-A) is a fourth-generation fluoroquinolone antibiotic.

Besifloxacin Hydrochloride

Besifloxacin Hydrochloride

🥰Excellent
Purity: 99.95%
Catalog No. T6406Alias BOL-303224-A, Besivance hydrochloride, Besifloxacin HClCas No. 405165-61-9
Besifloxacin Hydrochloride (BOL-303224-A) is a fourth-generation fluoroquinolone antibiotic.
Pack SizePriceAvailabilityQuantity
5 mg$32In Stock
10 mg$52In Stock
25 mg$98In Stock
50 mg$175In Stock
100 mg$335In Stock
200 mg$495In Stock
500 mg$789In Stock
1 mL x 10 mM (in DMSO)$44In Stock
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Purity:99.95%
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Product Introduction

Bioactivity
Description
Besifloxacin Hydrochloride (BOL-303224-A) is a fourth-generation fluoroquinolone antibiotic.
In vitro
Besifloxacin has effectively bactericidal activity against prevalent and drug-resistant pathogens. Besifloxacin is the most potent agent tested against gram-positive pathogens and anaerobes and is generally equivalent to comparator fluoroquinolones in activity against most gram-negative pathogens. Besifloxacin demonstrates potent, broad-spectrum activity, which is particularly notable against gram-positive and gram-negative isolates that are resistant to other fluoroquinolones and classes of antibacterial agents.
Kinase Assay
20 ng of purified human DDK, together with increasing concentrations of each DDK inhibitor is pre-incubated for 5 min. Then 10 μCi (γ)-32P ATP and 1.5 μM cold ATP are added in a buffer containing 50 mM Tris-HCl (pH 7.5), 10 mM MgCl2, and 1 mM DTT and incubated for 30 min at 30°C. The proteins are denatured in 1X Laemmli buffer at 100°C followed by SDS-PAGE and autoradiography on HyBlot CL film. DDK kinase activity is indicated by Auto-phosphorylation of DDK. 32P-labeled bands are quantified using ImageJ and the IC50 values are calculated using GraphPad.
AliasBOL-303224-A, Besivance hydrochloride, Besifloxacin HCl
Chemical Properties
Molecular Weight430.3
FormulaC19H21ClFN3O3·HCl
Cas No.405165-61-9
SmilesC1CCN(C[C@@H](C1)N)c1c(cc2c(c1Cl)n(cc(c2=O)C(=O)O)C1CC1)F.Cl
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 11 mg/mL (25.56 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3240 mL11.6198 mL23.2396 mL116.1980 mL
5 mM0.4648 mL2.3240 mL4.6479 mL23.2396 mL
10 mM0.2324 mL1.1620 mL2.3240 mL11.6198 mL
20 mM0.1162 mL0.5810 mL1.1620 mL5.8099 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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