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BDA-366

现货
Catalog No.
B5978
BCL2 BH4 结构域的选择性拮抗剂
组合的产品项目
规格价格库存 数量
5mg
¥ 4,200.00
Ship with 10-15 days
25mg
¥ 14,400.00
Ship with 10-15 days

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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.

Chemical Properties

StorageStore at -20°C
M.Wt 423.50
Cas No.1909226-00-1
FormulaC24H29N3O4
SolubilitySoluble in DMSO
Chemical Name1-(((S)-3-(diethylamino)-2-hydroxypropyl)amino)-4-(((S)-oxiran-2-ylmethyl)amino)anthracene-9,10-dione
SDFDownload SDF
Canonical SMILESCCN(CC)C[C@@H](O)CNC1=CC=C(NC[C@@H]2OC2)C3=C1C(C4=C(C3=O)C=CC=C4)=O
运输条件试用装:蓝冰运输。 其他可选规格:常温运输或根据您的要求用蓝冰运输。
一般建议为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。

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批次:

化学结构

BDA-366