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BDA-366 Selective antagonist of BCL2 BH4 domain

Catalog No.B5978
Size Price Stock Qty
5mg
$350.00
In stock
25mg
$1,200.00
In stock

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Sample solution is provided at 25 µL, 10mM.

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Chemical structure

BDA-366

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Chemical Properties

Cas No. SDF Download SDF
Chemical Name 1-(((S)-3-(diethylamino)-2-hydroxypropyl)amino)-4-(((S)-oxiran-2-ylmethyl)amino)anthracene-9,10-dione
Canonical SMILES CCN(CC)C[[email protected]@H](O)CNC1=CC=C(NC[[email protected]@H]2OC2)C3=C1C(C4=C(C3=O)C=CC=C4)=O
Formula C24H29N3O4 M.Wt 423.50
Solubility Soluble in DMSO Storage Store at -20°C
Shipping Condition Evaluation sample solution : ship with blue ice.All other available size: ship with RT , or blue ice upon request
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Background

BDA-366 is a selective antagonist of BCL2 BH4 domain with Ki value of 3.3 nM [1].

BCL2 is an important anti-apoptotic protein. BCL2 homology 4 (BH4) domain is required for its antiapoptotic function, thus acts as a promising anticancer target [1].

BDA-366 is a selective BCL2 inhibitor. BDA-366 induced conformational change of BCL2 that exposed the BH3 domain, resulting in abrogation of its prosurvival function and conversion of BCL2 to a prodeath protein. In non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) cells, BDA-366 selectively bound to BCL2 with high affinity. BDA-366 induced apoptosis by BCL2-dependent BAX activation and cytochrome c release. In H460 cells, BDA-366 reduced Bcl2/IP3R binding, which then increased Ca2+ release [1].

In mice bearing H460 lung cancer xenografts, treatment with BDA-366 (0, 10, 20, and 30 mg/kg/day) via i.p. route for 14 days induced apoptosis and potently inhibited tumor growth in a dose-dependent way. There was no significant toxicity at the maximum therapeutic dose. In tumor tissue from patients with NSCLC, BDA-366 synergized with RAD001 and resulted in significantly greater inhibition of lung cancer growth compared with either agent alone [1].

Reference:
[1].  Han B, Park D, Li R, et al. Small-Molecule Bcl2 BH4 Antagonist for Lung Cancer Therapy. Cancer Cell, 2015, 27(6): 852-863.