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货期:询盘
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MedChemExpress LLC
- CAS号:
1391107-54-2
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询盘
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BM 957
CAS No. : 1391107-54-2
MCE 国际站:BM 957
产品活性:BM 957 是 Bcl-2 和Bcl-xL 的有效抑制剂,其 Ki 值分别为 1.2,<1 nM,IC50 值分别为 5.4,6.0 nM。
研究领域:Apoptosis
作用靶点:Bcl-2 Family
In Vitro: BM 957 (Compound 30) with ethyl and compound 31 with isopropyl bind to both Bcl-2 and Bcl-xL with very high affinities. While BM 957 and 31 bind to Bcl-2 with IC50 values of 5.4 and 4.0 nM, respectively (Ki values=1.2 and 0.8 nM, respectively), they bind to Bcl-xL with IC50 values of 6.0 and 3.9 nM, respectively (Ki values < 1 nM). BM 957 has IC50 values of 21 nM and 22 nM, respectively, in these two cancer cell lines (H1417 and H146 cell lines). All these compounds induce cell death in a dose-dependent manner but have different potencies. While BM 957 and 31 are several times more potent than 1 and 2. BM 957 at 10 nM, 28 at 100 nM and 2 at 30 nM all induce clear cleavage of PARP and activation of caspase-3 and have similar effects. Hence, the potencies for these three compounds in induction of cleavage of PARP and activation of caspase-3 in the H146 cells are consistent with their potencies in induction of cell death.
In Vivo: It is found that 28 at 50 mg/kg, BM 957 at 25 mg/kg and 31 at 10 mg/kg, daily, intravenous dosing, 5 days a week for 2 weeks are well tolerated in SCID mice and the animals have less than 10% of weight loss. Higher doses of these compounds (75 mg/kg for 28, 50 mg/kg for 30 and 25 mg/kg for 31) cause more than 10% of weight loss. Mice bearing H146 tumors are given a single i.v. dose of 28 at 50 mg/kg or BM 957 at 25 mg/kg. It showed that although compound 28 at 50 mg/kg effectively inhibits tumor growth, it fails to induce tumor regression. In contrast, BM 957 at 25 mg/kg is capable of achieving complete tumor regression. Of 7 mice treated with BM 957, all mice are tumor-free at day 47 and five (71%) remained tumor-free on day 58. Similar to the data obtained from our MTD experiment, both compounds 28 and BM 957 are well tolerated in tumor-bearing animals. All treated animals experienced less than 10% weight loss compared to the vehicle control and all regained their weight quickly after the treatments are finished. This in vivo experiment thus establish that BM 957 achieves complete and durable tumor regression in the H146 xenograft tumor model and is more efficacious than 28.
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文献和实验Histologic analysis of murine BM is a necessary complement to flow cytometric or in vitro analysis. Techniques to do this are well established in human hematopathology. A long tradition in experimental hematology focuses on femur
Analysis of murine BM: specimen choice, sampling and processing.
Histologic analysis of murine BM is a necessary complement to flow cytometric or in vitro analysis. Techniques to do this are well established in human hematopathology. A long tradition in experimental hematology focuses on femur
1、反光显微镜构造及各部件的认识 反光显微镜(也称金相显微镜)样式很多,原理相同,都是通过自试样表面的反射光束来观察分析制品的显微结构,图1是上海光学仪器五厂生产的BM12透反两用正置金相显微镜。 反光显微镜的构造除了与偏光显微镜有相似的镜座、镜臂、镜筒、目镜、物镜及物台等主要部件外,还有一个垂直照明器。 图1 BM12透反两用正置金相显微镜 (1) 目镜;(2)光源、灯泡;(3)物镜;(4)物台
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