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BH3I-1

Chemical Structure : BH3I-1

CAS No.: 300817-68-9

BH3I-1 (BHI1, BHI-1, BHI 1;BH 3I1)

Catalog No.: PC-42125Not For Human Use, Lab Use Only.

BH3I-1 (BHI1) is a small-molecule Bcl-2 antagonist that inhibits the ineraction of Bak BH3 and Bcl-xL with Ki of 2.4 uM in FP binding assay.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

BH3I-1 (BHI1) is a small-molecule Bcl-2 antagonist that inhibits the ineraction of Bak BH3 and Bcl-xL with Ki of 2.4 uM in FP binding assay.
BH3I-1 (BHI1) specifically blocks the BH3-domain-mediated heterodimerization between Bcl-2 family members in vitro and in vivo and induces apoptosis.
BH3I-1 (BHI1) also potently inhibits p53/hDM2 with Kd of 5.3 uM.

Physicochemical Properties

M.Wt 400.3105
Formula C15H14BrNO3S2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 3.9 mg/mL

Chemical Name/SMILES

3-Thiazolidineacetic acid, 5-[(4-bromophenyl)methylene]-α-(1-methylethyl)-4-oxo-2-thioxo-

References

1. Degterev A, et al. Nat Cell Biol. 2001 Feb;3(2):173-82.

2. Wang L, et al. Bioorg Med Chem Lett. 2008 Jan 1;18(1):236-40.

3. Porter JR, et al. Chem Commun (Camb). 2010 Nov 14;46(42):8020-2.

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