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BH3I-1 (BHI1) is a Bcl-2 antagonist.

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 2 mg | $35 | In Stock | |
| 5 mg | $54 | In Stock | |
| 10 mg | $89 | In Stock | |
| 25 mg | $168 | In Stock | |
| 50 mg | $277 | In Stock | |
| 100 mg | $449 | In Stock | |
| 200 mg | $649 | In Stock |
| Description | BH3I-1 (BHI1) is a Bcl-2 antagonist. |
| Targets&IC50 | MDM2-p53:5.3 μM(Kd), BH3-BCL XL:2.4 μM(Ki) |
| In vitro | BH3I-1 inhibits Bcl-xL heterodimerization in vitro. It also induces cytochrome c release[1]. BH3I-1, while inhibiting its reported target Bcl-2/Bim and Bcl-xL/Bim, shows significant inhibition of both the p53/hDM2 and p300/Hif-1a interactions[2]. |
| Cell Research | Cells (5×104 cells per well) are seeded into white 96-well plates (Costar) and treated with various concentrations of the compounds for 48 h. For zVAD-FMK protection experiments, cells are preincubated with 100 μM zVAD-FMK for 1 h before the addition of chemicals. Cell viability is determined with an MTS assay. For PI staining experiments, cells are grown in 24-well plates and then incubated with 2 μg ml/L PI. Cell death is determined by FACS analysis.(Only for Reference) |
| Synonyms | BHI1 |
| Molecular Weight | 400.31 |
| Formula | C15H14BrNO3S2 |
| Cas No. | 300817-68-9 |
| Smiles | CC(C)C(N1C(=S)S\C(=C\c2ccc(Br)cc2)C1=O)C(O)=O |
| Relative Density. | no data available |
| Color | Yellow |
| Appearance | solid |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||||||||||||
| Solubility Information | H2O: < 1 mg/mL (insoluble or slightly soluble) DMSO: 60 mg/mL (149.88 mM), Sonication is recommended. Ethanol: 11 mg/mL (27.48 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||||||||||||
Ethanol/DMSO
DMSO
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