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Pentachloropseudilin

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Catalog No. T24612Cas No. 69640-38-6
Alias PClP, Antibiotic A 15104 Y

Pentachloropseudilin (PClP) is a reversible variant 1 myosin inhibitor with antimicrobial activity that inhibits Myo1s and class 5 myosins.Pentachloropseudilin inhibits growth factor-beta (TGF-β), which blocks host cell invasion by Trypanosoma cruzi.

Pentachloropseudilin

Pentachloropseudilin

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Purity: 98.14%
Catalog No. T24612Alias PClP, Antibiotic A 15104 YCas No. 69640-38-6
Pentachloropseudilin (PClP) is a reversible variant 1 myosin inhibitor with antimicrobial activity that inhibits Myo1s and class 5 myosins.Pentachloropseudilin inhibits growth factor-beta (TGF-β), which blocks host cell invasion by Trypanosoma cruzi.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$1,5206-8 weeks6-8 weeks
50 mg$1,9806-8 weeks6-8 weeks
100 mg$2,5006-8 weeks6-8 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.14%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Pentachloropseudilin (PClP) is a reversible variant 1 myosin inhibitor with antimicrobial activity that inhibits Myo1s and class 5 myosins.Pentachloropseudilin inhibits growth factor-beta (TGF-β), which blocks host cell invasion by Trypanosoma cruzi.
In vitro
Pentachloropseudoprotein (PCLP) inhibits TGF-β-stimulated Smad2/3 phosphorylation and activation of the plasminogen activator inhibitor-1 (PAI-1) promoter, with an IC50 value of 0.1 μM in target cells (A549, HepG2, and Mv1Lu cells) [2].
Pentachloropseudoprotein reduced TGF-β-stimulated expression of waveform protein, N-adhesin, and fibronectin, thereby blocking TGF-β-induced epithelial-to-mesenchymal transition (EMT) in these cells. Pentachloropseudoprotein (0.05 to 1 μΜ; 0-6 hours) pretreatment inhibited the TGF-β-mediated increase in p-Smad2/3 expression (50 or 100 pM), reducing it by 47% (Mv1Lu) and 79% (A549), respectively [2].
Sucrose density gradient analysis and immunofluorescence staining showed that pentachloro pseudilin (0.2 μM) inhibited TGF-β-stimulated cellular responses by accelerating caveolae-mediated internalization, inhibiting cell surface type II TGF-β receptor expression, and then degrading the receptor primarily through lysosome-dependent degradation [2].
SynonymsPClP, Antibiotic A 15104 Y
Chemical Properties
Molecular Weight331.41
FormulaC10H4Cl5NO
Cas No.69640-38-6
SmilesOc1c(Cl)cc(Cl)cc1-c1[nH]c(Cl)c(Cl)c1Cl
Relative Density.1.733g/cm3
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight | 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 (241.39 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 3.3 mg/mL (9.96 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0174 mL15.0871 mL30.1741 mL150.8705 mL
5 mM0.6035 mL3.0174 mL6.0348 mL30.1741 mL
10 mM0.3017 mL1.5087 mL3.0174 mL15.0871 mL
20 mM0.1509 mL0.7544 mL1.5087 mL7.5435 mL
50 mM0.0603 mL0.3017 mL0.6035 mL3.0174 mL
100 mM0.0302 mL0.1509 mL0.3017 mL1.5087 mL

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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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