CAS NO: | 331244-89-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | BAM7 is a direct and selective activator of proapoptoticBAXwith anIC50of 3.3 μM. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | BAM7 is selective for the BH3-binding site on BAX. BAM7 activates BAX and BAX-dependent cell death. Whereas treatment with BAX or BAM7 alone has no effect on the liposomes, the combination of BAM7 and BAX yields dose-responsive liposomal release of entrapped fluorophore. BAM7 dose- and time-responsively impairs the viability ofBak-/-MEFs that exclusively express BAX but has no effect onBak-/-MEFs that contain BAK but lack BAX. In contrast, standard proapoptotic stimuli such as serum withdrawal, Staurosporine and Etoposide induces an equivalent apoptotic response inBax-/-andBak-/-MEFs. As further evidence of BAM7 specificity of action, (i) BAM7 does not affect the viability ofBax-/-Bak-/-MEFs; (ii) ANA-BAM16, which does not bind or activate BAX, has no effect onBak-/-MEFs; and (iii) BAM7 selectively induces cell death ofBax-/-Bak-/-MEFs reconstituted with wild-type BAX but not BAXK21E , which bears the mutation that abrogates BAM7 binding[1]. | ||||||||||||||||
分子量 | 405.47 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H19N5O2S | ||||||||||||||||
CAS 号 | 331244-89-4 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 5 mg/mL(12.33 mM;Need ultrasonic) 配制储备液
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