BDA-366 是一种有效的Bcl2拮抗剂 (Ki= 3.3 nM)，对 Bcl2-BH4 结构域具有较高的亲和力和选择性。BDA-366 诱导 Bcl2 的构象改变，从而消除其抗凋亡功能，将 Bcl2 从存活分子转化为细胞死亡诱导因子。BDA-366 可抑制肺癌细胞生长。
| 生物活性 | BDA-366 is a potentBcl2antagonist (Ki= 3.3 nM), binding Bcl2-BH4 domain with high affinity and selectivity. BDA-366 induces conformational change in Bcl2 that abrogates its antiapoptotic function, converting it from a survival molecule to a cell death inducer. BDA-366 suppresses growth of lungcancercells[1]. |
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| 运输条件 | Room temperature in continental US; may vary elsewhere. |
| 储存方式 | Please store the product under the recommended conditions in the Certificate of Analysis. |
