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Cephalexin hydrochloride

(Synonyms: Cephacillin hydrochloride, Cefalexin hydrochloride) Copy Product Info
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Synonyms: Cephacillin hydrochloride, Cefalexin hydrochloride

Catalog No. T22643 Copy Product Info
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Cephalexin hydrochloride is a potent, orally active semisynthetic cephalosporin compound with a broad antibacterial spectrum. Cephalexin hydrochloride exhibits antibacterial activity against a wide range of gram-positive and gram-negative bacterial species. Cephalexin hydrochloride targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin hydrochloride is utilized in investigations involving pneumonia, streptococcal pharyngitis, bacterial endocarditis, and bacterial cell wall biosynthesis mechanisms.
Pack SizePriceUSA StockGlobal StockQuantity
10 mg$29-In Stock
50 mgPreferential-In Stock
1 mL x 10 mM (in DMSO)$41-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Cephalexin hydrochloride is a potent, orally active semisynthetic cephalosporin compound with a broad antibacterial spectrum. Cephalexin hydrochloride exhibits antibacterial activity against a wide range of gram-positive and gram-negative bacterial species. Cephalexin hydrochloride targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin hydrochloride is utilized in investigations involving pneumonia, streptococcal pharyngitis, bacterial endocarditis, and bacterial cell wall biosynthesis mechanisms.
In vitro
Cephalexin hydrochloride (10μg/mL) disrupts polymer peptidoglycan (PG) biogenesis through the inactivation of enzymes known as penicillin-binding proteins (PBPs)[1]. Cephalexin hydrochloride exhibits inhibitory activity against a broad spectrum of Gram-positive and Gram-negative organisms, with MIC values of 2, 2, 2, 2, 4, 4.4, and 5.7 μg/mL for Bacillus anthracis, Edwardsiella tarda, Vibrio cholerae, Pasteurella multocida, Edwardsiella tarda, Alcaligenes sp., and Proteus rettgeri, respectively[2].
In vivo
Cephalexin hydrochloride (0-50 mg/kg; p.o.; 3.5 h) has antibacterial activity (Streptococcus pyogenes, Streptococcus pneumoniae, Staphylococcus aureus and several gram-negative) in male Swiss-Webster mice with infected bacterial[2].
SynonymsCephacillin hydrochloride, Cefalexin hydrochloride
Chemical Properties
Molecular Weight383.85
FormulaC16H18ClN3O4S
Cas No.59695-59-9
SmilesO=C1N2[C@@]([C@@H]1NC([C@H](N)C3=CC=CC=C3)=O)(SCC(C)=C2C(O)=O)[H].Cl
Relative Density.no data available
Storage & Solubility Information
StorageKeep away from moisture, Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (208.41 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6052 mL13.0259 mL26.0518 mL130.2592 mL
5 mM0.5210 mL2.6052 mL5.2104 mL26.0518 mL
10 mM0.2605 mL1.3026 mL2.6052 mL13.0259 mL
20 mM0.1303 mL0.6513 mL1.3026 mL6.5130 mL
50 mM0.0521 mL0.2605 mL0.5210 mL2.6052 mL
100 mM0.0261 mL0.1303 mL0.2605 mL1.3026 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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:
mg/kg
g
µL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

Keywords

Related Tags: Cephalexin hydrochloride chemical structure | Cephalexin hydrochloride in vivo | Cephalexin hydrochloride in vitro | Cephalexin hydrochloride formula | Cephalexin hydrochloride molecular weight