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Ciprofloxacin monohydrochloride

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Catalog No. T0250Cas No. 93107-08-5
Alias Ciprofloxacin hydrochloride, Ciprofloxacin HCl, Bay-09867 (hydrochloride)

Ciprofloxacin monohydrochloride (Bay-09867 hydrochloride) is a broad-spectrum antimicrobial carboxyfluoroquinoline.

Ciprofloxacin monohydrochloride

Ciprofloxacin monohydrochloride

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Purity: 99.73%
Catalog No. T0250Alias Ciprofloxacin hydrochloride, Ciprofloxacin HCl, Bay-09867 (hydrochloride)Cas No. 93107-08-5
Ciprofloxacin monohydrochloride (Bay-09867 hydrochloride) is a broad-spectrum antimicrobial carboxyfluoroquinoline.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 g$35-In Stock
5 g$73-In Stock
10 g$106-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.73%
Appearance:Solid
Color:White
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Product Introduction

Ciprofloxacin monohydrochloride AI Summary
Ciprofloxacin monohydrochloride exhibits broad-spectrum antibacterial activity against a variety of gram-positive and gram-negative bacteria, including drug-resistant strains. It is effective against notable pathogens such as Staphylococcus aureus, Streptococcus species, Enterococcus faecium, Escherichia coli, Pseudomonas aeruginosa, Listeria monocytogenes, Klebsiella pneumoniae, Klebsiella oxytoca, Bacillus anthracis, and Salmonella enterica, with Minimum Inhibitory Concentrations (MIC) ranging from 0.05 to 6.25 µg/mL. It also shows significant antifungal activity, particularly against Candida albicans. In vitro studies reveal that Ciprofloxacin monohydrochloride inhibits Escherichia coli DNA gyrase with an IC50 of 0.2-0.24 µg/mL and demonstrates inhibitory effects on DNA, RNA, and protein synthesis in bacterial cells. It exhibits oral bioavailability in rats at 16% and shows favorable pharmacokinetic properties, including moderate oral bioavailability and good plasma exposure levels. Additionally, Ciprofloxacin monohydrochloride has been noted for its activity in blocking Ebola virus entry and inhibiting human tyrosyl-DNA phosphodiesterase 1 (TDP1). In vivo studies indicate its efficacy against bacterial infections following subcutaneous and oral administrations, highlighting its therapeutic potential..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Ciprofloxacin monohydrochloride (Bay-09867 hydrochloride) is a broad-spectrum antimicrobial carboxyfluoroquinoline.
SynonymsCiprofloxacin hydrochloride, Ciprofloxacin HCl, Bay-09867 (hydrochloride)
Chemical Properties
Molecular Weight367.80
FormulaC17H18FN3O3·HCl
Cas No.93107-08-5
SmilesCl.OC(=O)C1=CN(C2CC2)C2=CC(N3CCNCC3)=C(F)C=C2C1=O
Relative Density.no data available
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 4.23 mg/mL (11.5 mM), Sonication is recommended.
H2O: 30.03 mg/mL (81.65 mM), Sonication is recommended.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.7189 mL13.5943 mL27.1887 mL135.9434 mL
5 mM0.5438 mL2.7189 mL5.4377 mL27.1887 mL
10 mM0.2719 mL1.3594 mL2.7189 mL13.5943 mL
H2O
1mg5mg10mg50mg
20 mM0.1359 mL0.6797 mL1.3594 mL6.7972 mL
50 mM0.0544 mL0.2719 mL0.5438 mL2.7189 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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%
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