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HGC652
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Catalog No. T204670Cas No. 3055558-98-7
HGC652 is a molecular glue targeting E3 ubiquitin ligase TRIM21 (KD=0.061 µM), promoting its formation of a ternary complex with NUP98 to induce degradation of NUP155 and nuclear pore complex proteins. HGC652 inhibits proliferation and induces cell death in multiple cancer cell lines.
HGC652
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Purity: 99.95%
Catalog No. T204670Cas No. 3055558-98-7
HGC652 is a molecular glue targeting E3 ubiquitin ligase TRIM21 (KD=0.061 µM), promoting its formation of a ternary complex with NUP98 to induce degradation of NUP155 and nuclear pore complex proteins. HGC652 inhibits proliferation and induces cell death in multiple cancer cell lines.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $84 | - | In Stock | |
| 5 mg | $198 | - | In Stock | |
| 10 mg | $328 | - | In Stock | |
| 25 mg | $668 | - | In Stock | |
| 50 mg | $1,070 | - | In Stock | |
| 100 mg | $1,720 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.95%
Appearance:Solid
Color:White
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | HGC652 is a molecular glue targeting E3 ubiquitin ligase TRIM21 (KD=0.061 µM), promoting its formation of a ternary complex with NUP98 to induce degradation of NUP155 and nuclear pore complex proteins. HGC652 inhibits proliferation and induces cell death in multiple cancer cell lines. |
| Targets&IC50 | PANC1 cells viability:0.094 μM, TRIM21:0.061 µM (Kd) |
| In vitro | HGC652 (72h) exhibited growth inhibition in PANC-1 cells (transfected with TRIM21 siRNA), with an IC50 of 0.094 μM. For eight other cancer cell lines, HGC652 (72h) showed IC50 values ranging from 0.106 to 0.822 μM[1]. HGC652 (0.5/5 μM; 24h) induced significant degradation of NUP155 and GLE1 proteins in PANC-1 cells [1]. |
| Molecular Weight | 449.6 |
| Formula | C23H28FNO3S2 |
| Cas No. | 3055558-98-7 |
| Smiles | O=C(C=1C=CC(=CC1S(=O)(=O)C)C2=CC=C(F)C=C2SC)N(C)CC3CCCCC3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 50.00 mg/mL (111.21 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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