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BH3I-1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
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BH3I-1 是一种 Bcl-2 家族拮抗剂,可抑制 Bak BH3 肽与 Bcl-xL 的结合,在 FP 测定中的 Ki 为 2.4±0.2 μM。 BH3I-1 对 p53/MDM2 对的 Kd 为 5.3 μM。

Cell experiment:

Jurkat cells overexpressing Bcl-xL, FL 5.12 and FL 5.12/Bcl-xL cells (5×104 cells per well) are seeded into white 96-well plates and treated with various concentrations of the compounds (e.g., BH3I-1; 30 μM and 90 μM)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 with a Victor plate reader. For PI staining experiments, cells are grown in 24-well plates and then incubated with 2 μg/mL PI. Cell death is determined by FACS analysis in a FACSCalibur machine[3].

产品描述

IC50: 293.95 μM

BH3I-1 is an inhibitor of Bcl-2 or Bcl-XL.

It has been reported that a disregulation of the Bcl-2/ Bcl-XL family proteins may result in the development of cancer, since the failure of the inactivation of pro-apoptotic pathways, or the activation of anti-apoptotic pathways, may occur in the regulation processes.

In vitro: The Bcl-2 inhibitors BH3I-1 and it analog BH3I-2 had been applied as lead compounds to find possible Bcl-2 or Bcl-X(L) inhibitors by using computer-assisted screening of in-house database. The identified compounds were further studied regarding their possible application as a drug. It was found that the induction of apoptosis, which was shown as number of hypodiploid cells, was increased by adding BH3I-1 and it analog BH3I-2 to Bjab Bcl-XL and Bjab neo/mock cells. In addition, the effects of the pro-apoptotic proteins Bax and Bak on the induction of apoptosis via BH3I-1 and it analog BH3I-2 were investigated with a variety of knockout cell lines, and resulted showed that the presence or absence of Bak or Bax has no significant influence on the amount of apoptotic events induced by BH3I-1 and it analog BH3I-2 [1].

In vivo: Currently, there is no animial in vivo data reported.

Clinical trial: Up to now, BH3I-1 is still in the preclinical development stage.

Reference:
[1] Füllbeck M,Gebhardt N,Hossbach J,Daniel PT,Preissner R.  Computer-assisted identification of small-molecule Bcl-2 modulators. Comput Biol Chem.2009 Dec;33(6):451-6.

 
 
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