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BCL6-IN-3

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Catalog No. T10487Cas No. 2253878-44-1

BCL6-IN-3 is a potent BCL6 inhibitor with GI50 of 70 nM in SU-DHL4 cells. BCL6-in-3 regulates cell activation, differentiation, DNA damage and apoptosis, and has antitumor activity.

BCL6-IN-3

BCL6-IN-3

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Purity: 98.17%
Catalog No. T10487Cas No. 2253878-44-1
BCL6-IN-3 is a potent BCL6 inhibitor with GI50 of 70 nM in SU-DHL4 cells. BCL6-in-3 regulates cell activation, differentiation, DNA damage and apoptosis, and has antitumor activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$117In StockIn Stock
5 mg$268In StockIn Stock
10 mg$395In StockIn Stock
25 mg$592In StockIn Stock
50 mg$828In StockIn Stock
100 mg$1,130In StockIn Stock
500 mgPreferential-In Stock
1 mL x 10 mM (in DMSO)$412In 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:98.17%
Appearance:Solid
Color:White
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Product Introduction

BCL6-IN-3 AI Summary
BCL6-IN-3 demonstrates significant potential as a BCL6 inhibitor, exhibiting an IC50 of 520.0 nM for human BCL6 inhibition. It effectively induces degradation of BCL6 in various human cell lines, with DC50 values ranging between 0.049 µM and 0.09 µM. The compound shows antiproliferative activity against multiple human cell lines, with GI50 values from 35.0 nM to 1600.0 nM. It also displays good kinetic solubility in HEPES and PBS buffers and possesses a metabolic stability with a clearance rate of 78.0 mL·min⁻¹·g⁻¹ in CD-1 mouse liver microsomes. BCL6-IN-3 has a log D value of 4.3, indicating its lipophilicity, and shows good oral bioavailability at 54.0% in BALB/c mice. Additional pharmacokinetic parameters include a short half-life of 1.4 hours and a moderate volume of distribution at steady state of 2.1 L·kg⁻¹. Furthermore, the compound has high protein binding with 99.96% bound to plasma proteins in BALB/c mice. These attributes highlight BCL6-IN-3's potential in therapeutic applications targeting BCL6 with promising bioavailability and solubility profiles..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
BCL6-IN-3 is a potent BCL6 inhibitor with GI50 of 70 nM in SU-DHL4 cells. BCL6-in-3 regulates cell activation, differentiation, DNA damage and apoptosis, and has antitumor activity.
Targets&IC50
Proliferation (SU-DHL4 cells):70 nM (GI50)
Chemical Properties
Molecular Weight508.99
FormulaC24H31ClF2N6O2
Cas No.2253878-44-1
SmilesC(CC(C)(C)O)N1C=2C(N(C)C1=O)=CC=C(NC3=NC(=NC=C3Cl)N4C[C@H](C)C(F)(F)[C@H](C)C4)C2
Relative Density.1.38 g/cm3 (Predicted)
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: 180 mg/mL (353.64 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9647 mL9.8234 mL19.6468 mL98.2338 mL
5 mM0.3929 mL1.9647 mL3.9294 mL19.6468 mL
10 mM0.1965 mL0.9823 mL1.9647 mL9.8234 mL
20 mM0.0982 mL0.4912 mL0.9823 mL4.9117 mL
50 mM0.0393 mL0.1965 mL0.3929 mL1.9647 mL
100 mM0.0196 mL0.0982 mL0.1965 mL0.9823 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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