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Sarafloxacin hydrochloride

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Catalog No. T1107Cas No. 91296-87-6
Alias Sarafloxacin HCl, A-56620 HCl, A-56620 (hydrochloride)

Sarafloxacin hydrochloride (A-56620 (hydrochloride)), a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.

Sarafloxacin hydrochloride

Sarafloxacin hydrochloride

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Purity: 97.44%
Catalog No. T1107Alias Sarafloxacin HCl, A-56620 HCl, A-56620 (hydrochloride)Cas No. 91296-87-6
Sarafloxacin hydrochloride (A-56620 (hydrochloride)), a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 mg$35-In Stock
1 mL x 10 mM (in DMSO)$39In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:97.44%
Appearance:Solid
Color:White
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Product Introduction

Sarafloxacin hydrochloride AI Summary
Sarafloxacin hydrochloride exhibits potent in vitro antibacterial activity against a wide range of bacteria, including Staphylococcus aureus, Staphylococcus epidermis, Streptococcus faecium, Streptococcus pyogenes, Escherichia coli, Enterobacter aerogenes, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter, with minimal inhibitory concentrations (MIC) ranging from 0.02 to 1.56 µg/mL. The compound also demonstrates significant in vivo antibacterial efficacy against systemic infections by Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa in mice, with effective dose (ED50) values ranging from 0.6 to 21.4 mg/kg when administered subcutaneously or orally. Additionally, Sarafloxacin hydrochloride shows inhibition against various enzyme and receptor targets, including Lamin A splicing, HSD17B4, JMJD2E, ALDH1A1, HPGD, and the vitamin D receptor (VDR), with potencies ranging from 2238.7 nM to 100000.0 nM. It also acts as a delayed death inhibitor of the malarial parasite plastid and inhibits human tyrosyl-DNA phosphodiesterase 1 (TDP1) under varying conditions, with potencies between 14581.0 nM and 23715.0 nM. Furthermore, Sarafloxacin hydrochloride exhibits antiviral properties, including inhibition of SARS-CoV-2 induced cytotoxicity in Caco-2 and VERO-6 cells at 10 µM concentration after 48 hours, as well as protease inhibition against the SARS-CoV-2 3CL-Pro protease, although these activities show variable inhibition percentages. The compound also demonstrates the ability to inhibit sodium fluorescein uptake in OATP1B1- and OATP1B3-transfected CHO cells with inhibition rates of 109.55% and 115.57%, respectively, at an equimolar concentration of 10 µM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Sarafloxacin hydrochloride (A-56620 (hydrochloride)), a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.
SynonymsSarafloxacin HCl, A-56620 HCl, A-56620 (hydrochloride)
Chemical Properties
Molecular Weight421.83
FormulaC20H18ClF2N3O3
Cas No.91296-87-6
SmilesCl.OC(=O)C1=CN(C2=CC=C(F)C=C2)C2=CC(N3CCNCC3)=C(F)C=C2C1=O
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/Shipping at ambient temperature.
Solubility Information
DMSO: 5.5 mg/mL (13.04 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3706 mL11.8531 mL23.7062 mL118.5312 mL
5 mM0.4741 mL2.3706 mL4.7412 mL23.7062 mL
10 mM0.2371 mL1.1853 mL2.3706 mL11.8531 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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