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Prilocaine hydrochloride

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Catalog No. T0796Cas No. 1786-81-8
Alias Xylonest, Propitocaine hydrochloride, Prilocaine HCl

Prilocaine hydrochloride (Prilocaine HCl) is a local anesthetic of the amino amide type, binds to voltage-gated sodium ion channels in the neuronal membrane, thereby preventing the permeability of sodium ions.

Prilocaine hydrochloride

Prilocaine hydrochloride

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Purity: 99.97%
Catalog No. T0796Alias Xylonest, Propitocaine hydrochloride, Prilocaine HClCas No. 1786-81-8
Prilocaine hydrochloride (Prilocaine HCl) is a local anesthetic of the amino amide type, binds to voltage-gated sodium ion channels in the neuronal membrane, thereby preventing the permeability of sodium ions.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
100 mg$30In StockIn Stock
500 mg$68In StockIn Stock
1 g$98-In Stock
1 mL x 10 mM (in DMSO)$30In 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:99.97%
Appearance:Solid
Color:White
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Product Introduction

Prilocaine hydrochloride AI Summary
Prilocaine hydrochloride exhibits a broad spectrum of biological activities. It shows significant antiplasmodial activity against Plasmodium falciparum GB4 with an IC50 of 12589.25 nM, and a potency range of 11220.2-14125.4 nM for inhibiting Plasmodium falciparum proliferation. Additionally, it demonstrates potent inhibition of various targets including Lamin A Splicing (25118.9 nM), Tau Fibril Formation (8912.5 nM), HPGD (19952.6 nM), Human alpha-Glucosidase (3981.1 nM), Lipid Storage Modulation (4466.8 nM), beta-arrestin-biased ligands of beta2-adrenergic receptor (3162.3 nM), Eya2 Phosphatase (22387.2 nM), and Histone Lysine Methyltransferase G9a (22.4 nM). It also exhibits inhibitory activity in OATP1B1- and OATP1B3-transfected CHO cells (87.24% and 74.6% inhibition at 10 uM, respectively). Despite showing low activity against SARS-CoV-2 in some assays, it has demonstrated inhibition of SARS-CoV-2 induced cytotoxicity in Caco-2 cells (-29.5% inhibition at 10 uM) and VERO-6 cells (0.16% inhibition at 10 uM). Prilocaine hydrochloride also inhibits the SARS-CoV-2 3CL-Pro protease by 14.97% at 20µM. Additionally, the compound exhibits antifungal activity against Candida albicans and antibacterial activity against multiple strains, including Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and MRSA Staphylococcus aureus. Prilocaine hydrochloride is a multifaceted molecule with potential applications in antiplasmodial, antiviral, antifungal, antibacterial therapies, and modulating various biological pathways..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Prilocaine hydrochloride (Prilocaine HCl) is a local anesthetic of the amino amide type, binds to voltage-gated sodium ion channels in the neuronal membrane, thereby preventing the permeability of sodium ions.
SynonymsXylonest, Propitocaine hydrochloride, Prilocaine HCl
Chemical Properties
Molecular Weight256.77
FormulaC13H21ClN2O
Cas No.1786-81-8
SmilesCl.CCCNC(C)C(=O)Nc1ccccc1C
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: 60 mg/mL (233.67 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.8945 mL19.4727 mL38.9454 mL194.7268 mL
5 mM0.7789 mL3.8945 mL7.7891 mL38.9454 mL
10 mM0.3895 mL1.9473 mL3.8945 mL19.4727 mL
20 mM0.1947 mL0.9736 mL1.9473 mL9.7363 mL
50 mM0.0779 mL0.3895 mL0.7789 mL3.8945 mL
100 mM0.0389 mL0.1947 mL0.3895 mL1.9473 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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