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BT2 is a BCKDC kinase (BDK) inhibitor with an IC50 of 3.19 μM. BT2 binding to BDK triggers helix movements in the N-terminal domain, resulting in the dissociation of BDK from the branched-chain α-ketoacid dehydrogenase complex (BCKDC). BT2 (compound 4) is also a potent and selective Mcl-1 inhibitor with a Ki value of 59 μM.
规格 | 价格 | 促销价格 | 库存 |
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18817579266
实验数据
技术信息
CAS号 | 34576-94-8 | 储存条件 |
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分子式 | C9H4Cl2O2S | 运输 | 蓝冰 | |||
分子量 | 247.10 | 别名 | ||||
溶解度 |
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动物实验配方 |
生物活性