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SB 202190 hydrochloride

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Catalog No. T35592Cas No. 350228-36-3
Alias SB 202190 HCl

SB 202190 hydrochloride is the salt form of SB 202190.SB 202190 (FHPI) is a p38 MAPK inhibitor that inhibits p38α and p38β2 with selective, cell-permeable, and antitumor activity, and also induces differentiation of human embryonic stem cells to cardiomyocytes.

SB 202190 hydrochloride

SB 202190 hydrochloride

😃Good
Purity: 99.99%
Catalog No. T35592Alias SB 202190 HClCas No. 350228-36-3
SB 202190 hydrochloride is the salt form of SB 202190.SB 202190 (FHPI) is a p38 MAPK inhibitor that inhibits p38α and p38β2 with selective, cell-permeable, and antitumor activity, and also induces differentiation of human embryonic stem cells to cardiomyocytes.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$37In StockIn Stock
5 mg$59In StockIn Stock
10 mg$92In StockIn Stock
25 mg$148In StockIn Stock
50 mg$218In StockIn Stock
100 mg$325In StockIn Stock
200 mg$483-In Stock
1 mL x 10 mM (in DMSO)$65In 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:99.99%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
SB 202190 hydrochloride is the salt form of SB 202190.SB 202190 (FHPI) is a p38 MAPK inhibitor that inhibits p38α and p38β2 with selective, cell-permeable, and antitumor activity, and also induces differentiation of human embryonic stem cells to cardiomyocytes.
Targets&IC50
p38β2:100 nM (IC50), p38α:50 nM (IC50)
In vitro
Methods: SB 202190 hydrochloride (0-10 μM, 0-72 hours) was used to treat a subset of colorectal cancer (CRC) cell lines (RKO, CACO2, and SW480), and cell growth was measured.
Results: SB 202190 hydrochloride inhibited the growth of a subset of colorectal cancer (CRC) cell lines in a dose- and time-dependent manner. [1]
In vivo
Methods: SB 202190 hydrochloride (dissolved in 100% DMSO and then diluted with normal saline (NS) to a final DMSO concentration of 0.1%, injected intracerebroventricularly) was administered to rats, and both the VaD model group and the sham operation group received an equal volume of 0.1% DMSO injected ICV. Eight rats in each group were examined in the Morris water maze to assess spatial learning and memory, six rats were sacrificed and brain sections were prepared for TUNEL staining and Bcl-2/caspase-3 immunohistochemistry, and six rats were sacrificed and tissue homogenates were prepared for Western blot assay of phosphorylated p38 MAPK expression.
Results: Compared with the model group, the SB 202190 hydrochloride group showed a significantly shorter escape latency in the Morris water maze hidden platform test; compared with VaD model rats, the SB 202190 hydrochloride group also showed significantly reduced hippocampal neuronal apoptosis (P < 0.01) as well as higher (anti-apoptotic) Bcl-2 expression and lower (pro-apoptotic) caspase-3 expression. [2]
SynonymsSB 202190 HCl
Chemical Properties
Molecular Weight367.8
FormulaC20H15ClFN3O
Cas No.350228-36-3
SmilesCl.FC=1C=CC(=CC1)C=2NC(=NC2C=3C=CN=CC3)C=4C=CC(O)=CC4
Storage & Solubility Information
Storagestore at low temperature | Powder: -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 (163.13 mM), Sonication and heating are recommended.
DMF: 10 mg/mL (27.19 mM), Sonication and heating are recommended.
Ethanol:PBS (pH 7.2) (1:10): < 1 mg/mL, insoluble, Sonication is recommended.
Ethanol: 10 mg/mL (27.19 mM), Sonication and heating are recommended.
Solution Preparation Table
DMF/Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.7189 mL13.5943 mL27.1887 mL135.9434 mL
5 mM0.5438 mL2.7189 mL5.4377 mL27.1887 mL
10 mM0.2719 mL1.3594 mL2.7189 mL13.5943 mL
20 mM0.1359 mL0.6797 mL1.3594 mL6.7972 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:
% DMSO
%
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