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CSF1R-IN-3

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Catalog No. T64066Cas No. 2760584-90-3

CSF1R-IN-3 is an orally effective CSF-1R inhibitor with an IC50 value of 2.1 nM. CSF1R-IN-3 has anti-proliferative activity against colorectal cancer cells. CSF1R-IN-3 exhibits anti-tumour effects and immune enhancing effects by inhibiting the migration of macrophages and inducing the reprogramming of M2-type macrophages to M1-type macrophages, thus exhibited activity against colorectal cancer cells.

CSF1R-IN-3

CSF1R-IN-3

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🥰Excellent
Purity: 98.4%
Catalog No. T64066Cas No. 2760584-90-3
CSF1R-IN-3 is an orally effective CSF-1R inhibitor with an IC50 value of 2.1 nM. CSF1R-IN-3 has anti-proliferative activity against colorectal cancer cells. CSF1R-IN-3 exhibits anti-tumour effects and immune enhancing effects by inhibiting the migration of macrophages and inducing the reprogramming of M2-type macrophages to M1-type macrophages, thus exhibited activity against colorectal cancer cells.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$108In StockIn Stock
5 mg$272In StockIn Stock
10 mg$397In StockIn Stock
25 mg$738In StockIn Stock
50 mg$1,080In StockIn Stock
100 mg$1,550In StockIn Stock
1 mL x 10 mM (in DMSO)$343In StockIn Stock
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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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Purity:98.4%
Appearance:Solid
Color:Yellow
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Product Introduction

CSF1R-IN-3 AI Summary
CSF1R-IN-3 exhibits potent bioactivities, including the inhibition of CSF1R with an IC50 of 2.1 nM and a binding affinity characterized by a melting temperature (Tm) of 68.0 degrees Celsius and a dissociation constant (Kd) of 3.4 nM. It modulates macrophage reprogramming by reducing M2-like macrophages and increasing M1 macrophages. Additionally, it activates human CD4-positive and CD8-positive T cells in M2-macrophage culture medium. The compound induces apoptosis in both mouse MC38 cells and human HCT-116 cells when cultured with M2-macrophage medium. Furthermore, CSF1R-IN-3 demonstrates antitumor activity against mouse MC38 cells allografted in C57BL6 mice, showing significant tumor growth inhibition and modulating immune cell populations at various dosages..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
CSF1R-IN-3 is an orally effective CSF-1R inhibitor with an IC50 value of 2.1 nM. CSF1R-IN-3 has anti-proliferative activity against colorectal cancer cells. CSF1R-IN-3 exhibits anti-tumour effects and immune enhancing effects by inhibiting the migration of macrophages and inducing the reprogramming of M2-type macrophages to M1-type macrophages, thus exhibited activity against colorectal cancer cells.
Targets&IC50
CSF1R:2.1 nM
Chemical Properties
Molecular Weight574.67
FormulaC30H38N8O4
Cas No.2760584-90-3
SmilesCN1CCN(CC(=O)Nc2c(C)[nH]c(\C=C3/C(=O)Nc4cc(NC(=O)Nc5cc(on5)C(C)(C)C)ccc34)c2C)CC1
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: 56.2 mg/mL (97.8 mM), Sonication and heating to 60℃ are recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.7401 mL8.7006 mL17.4013 mL87.0065 mL
5 mM0.3480 mL1.7401 mL3.4803 mL17.4013 mL
10 mM0.1740 mL0.8701 mL1.7401 mL8.7006 mL
20 mM0.0870 mL0.4350 mL0.8701 mL4.3503 mL
50 mM0.0348 mL0.1740 mL0.3480 mL1.7401 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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