Bcl-2 Inhibitor II; YC137

Code: 197331-5MG D2-231

Biochem/physiol Actions

Reversible: no

Product does not compete with ATP.

Cell permeable: yes

Target Ki: 1.3 µM in binding Bcl-2


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€227.74 EACH
€227.74 inc. VAT

Biochem/physiol Actions

Reversible: no

Product does not compete with ATP.

Cell permeable: yes

Target Ki: 1.3 µM in binding Bcl-2

General description

A cell-permeable naphthoquinone compound that selectively induces apoptosis of Bcl-2-overexpressing cells (﹤300 nM in MDA-MB435B breast cancer cells) with little effect on a variety of primary cells, and Bcl-xL-dependent cells, even at a concentration of 5 µM. Preferentially binds Bcl-2 (Ki = 1.3 µM) and disrupts its interaction with Bid BH3, thereby blocking the anti-apoptotic activity of Bcl-2. Shown to induce the release of cytochrome c from mitochondria and activate caspase-9.

A cell-permeable molecule that targets the BH3 domain interaction and selectively induces apoptosis in Bcl-2-overexpressing cells (﹤300 nM in MDA-MB435B breast cancer cells). Exhibits little effect on a variety of primary cells and Bcl-xL-dependent cells, even at a concentrations as high as 5 µM. Inhibits the binding of Bid BH3 to Bcl-2 thereby blocking the anti-apoptotic activity of Bcl-2.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Other Notes

Real, P.J., et al. 2004. Cancer Res. 64, 7947.

Packaging

5 mg in Glass bottle

Packaged under inert gas

Warning

Toxicity: Carcinogenic / Teratogenic (D)

assay≥90% (HPLC)
colorred
formsolid
manufacturer/tradenameCalbiochem®
Quality Level100
shipped inwet ice
solubilityethanol: 5 mg/mL, DMSO: 5 mg/mL
storage conditionprotect from light, OK to freeze
storage temp.−20°C
Cas Number810659-53-1
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