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BDA-366

SKU: orb1300475

Description

BDA-366 is a high-affinity, selective antagonist of the Bcl-2 BH4 domain (Ki = 3.3 nM). It induces a pro-apoptotic conformational change, effectively inhibiting lung cancer cell growth in vitro, and shows potential for apoptosis research in oncology.

Research Area

Cell Biology

Images & Validation

Key Properties

CAS Number1909226-00-1
MW423.5
Purity99.46% (May vary between batches)
FormulaC24H29N3O4
SMILESN(C[C@H]1CO1)C2=C3C(=C(NC[C@@H](CN(CC)CC)O)C=C2)C(=O)C=4C(C3=O)=CC=CC4
TargetBcl-2 Family
SolubilityEthanol:5 mg/mL (11.81 mM);H2O:< 1 mg/mL (insoluble or slightly soluble);10% DMSO+40% PEG300+5% Tween-80+45% Saline:3.3 mg/mL (7.79 mM);DMSO:78 mg/mL (184.18 mM)

Bioactivity

Target IC50
Bcl-2:3.3 nM (Ki)
In Vitro
NSC 228155 promotes transactivation of several RTKs, including ErbB2 and ErbB3, Insulin R and IGF-1 R receptors in the cells. It stimulates dimerization of sEGFR domain II. NSC 228155 can rapidly move across cell membranes and disperse within both cytoplasmic and nuclear compartments. It rapidly generates hydrogen peroxide within cells. NSC 228155 is also a potent inhibitor of KIX-KID interaction(IC50 = 0.36 μM), but it is not particularly selective against CREB-mediated gene transcription in HEK 293T cells.

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Bcl2-BH4 domain, Bcl-2 Family, BDA-366, BDA366, BDA 366, Anticancer, Antiapoptotic function, Antitumor, Lung cancer, Inhibitor, inhibit

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Key Properties

No computed properties available.

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Protocol Information

BDA-366 (orb1300475)

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% DMSO +
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% Tween 80 +
%

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1 mg
$ 90.00
5 mg
$ 150.00
10 mg
$ 230.00
25 mg
$ 360.00
50 mg
$ 500.00
100 mg
$ 680.00
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