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Chem-0199

Catalog No. T213372 Copy Product Info
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Chem-0199 is an inhibitor of adipocyte enhancer-binding protein 1 (AEBP1). It disrupts the interaction between AEBP1 and CKAP4, which enhances antitumor immunity. Chem-0199 can inhibit Akt phosphorylation (p-Akt) and downregulate PD-L1 expression. It is applicable in cancer research, including studies on colorectal cancer.

Chem-0199

Copy Product Info
🥰Excellent
Catalog No. T213372

Chem-0199 is an inhibitor of adipocyte enhancer-binding protein 1 (AEBP1). It disrupts the interaction between AEBP1 and CKAP4, which enhances antitumor immunity. Chem-0199 can inhibit Akt phosphorylation (p-Akt) and downregulate PD-L1 expression. It is applicable in cancer research, including studies on colorectal cancer.

Chem-0199
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Chem-0199 is an inhibitor of adipocyte enhancer-binding protein 1 (AEBP1). It disrupts the interaction between AEBP1 and CKAP4, which enhances antitumor immunity. Chem-0199 can inhibit Akt phosphorylation (p-Akt) and downregulate PD-L1 expression. It is applicable in cancer research, including studies on colorectal cancer.
In vitro
Chem-0199 inhibits the binding of AEBP1 and CKAP4 in human and mouse cancer-associated fibroblasts (hCAFs/mCAFs). At concentrations of 10-100 μM, Chem-0199 suppresses Akt phosphorylation (p-Akt) and reduces PD-L1 expression in mCAFs. Furthermore, at doses of 10-100 μM over 48 hours, it significantly increases the ratio of IFN-γ+ and TNF-α+ CD8+ T cells in mouse spleens, restoring T cell cytotoxicity. Chem-0199 at 1-20 μM for 72 hours does not significantly inhibit the proliferation of various tumor cells (MC38, CT26, B16-F10).
In vivo
Chem-0199, when administered via intraperitoneal injection at doses ranging from 3 to 30 mg/kg, is capable of inhibiting the growth of MC38 tumors in wild-type C57BL/6 mice.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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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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