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Parsaclisib hydrochloride

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Catalog No. T28297Cas No. 1995889-48-9
Alias Parsaclisib HCl, INCB50465 HCl, INCB-50465, INCB050465 HCl, INCB-050465, INCB 50465, INCB 050465

Parsaclisib hydrochloride (INCB050465 HCl) is a selectve PI3Kδ inhibitor with antitumor activity. Parsaclisib demonstrates potent activity with IC50 values ranging from 0.2 to 2 nM.

Parsaclisib hydrochloride

Parsaclisib hydrochloride

Copy Product Info
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Catalog No. T28297Alias Parsaclisib HCl, INCB50465 HCl, INCB-50465, INCB050465 HCl, INCB-050465, INCB 50465, INCB 050465Cas No. 1995889-48-9
Parsaclisib hydrochloride (INCB050465 HCl) is a selectve PI3Kδ inhibitor with antitumor activity. Parsaclisib demonstrates potent activity with IC50 values ranging from 0.2 to 2 nM.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$1,2301-2 weeks1-2 weeks
50 mg$1,6101-2 weeks1-2 weeks
100 mg$2,5701-2 weeks1-2 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
Description
Parsaclisib hydrochloride (INCB050465 HCl) is a selectve PI3Kδ inhibitor with antitumor activity. Parsaclisib demonstrates potent activity with IC50 values ranging from 0.2 to 2 nM.
Targets&IC50
PI3Kδ:1 nM (IC50)
SynonymsParsaclisib HCl, INCB50465 HCl, INCB-50465, INCB050465 HCl, INCB-050465, INCB 50465, INCB 050465
Chemical Properties
Molecular Weight469.34
FormulaC20H23Cl2FN6O2
Cas No.1995889-48-9
SmilesCl.CCOc1c(cc(Cl)c(F)c1[C@@H]1CNC(=O)C1)[C@H](C)n1nc(C)c2c(N)ncnc12
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: 90 mg/mL (191.76 mM), Sonication is recommended.
H2O: Insoluble
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1307 mL10.6533 mL21.3065 mL106.5326 mL
5 mM0.4261 mL2.1307 mL4.2613 mL21.3065 mL
10 mM0.2131 mL1.0653 mL2.1307 mL10.6533 mL
20 mM0.1065 mL0.5327 mL1.0653 mL5.3266 mL
50 mM0.0426 mL0.2131 mL0.4261 mL2.1307 mL
100 mM0.0213 mL0.1065 mL0.2131 mL1.0653 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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