TMBIM6 antagonist-1
目录号: PL07564 纯度: ≥99%
CAS No. :123134-61-2
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中文名称
TMBIM6 antagonist-1
中文别名
1-(2-氨基苯基)-3-(3-硝基苯基)丙-2-烯-1-酮;1-(2-氨基苯基)-3-(3-硝基苯基)-2-丙烯-1-酮
英文名称
TMBIM6 antagonist-1
英文别名
2-Propen-1-one, 1-(2-aminophenyl)-3-(3-nitrophenyl)-;TMBIM6 antagonist-1;(2S)-3-[(2,5-Dihydro-5-oxoisoxazole)-2-yl]-2-aminopropanoic acid;BIA;β-(2,5-Dihydro-5-oxoisoxazole-2-yl)-L-alanine;1-(2-Aminophenyl)-3-(3-nitrophenyl)prop-2-en-1-one
Cas No.
123134-61-2
分子式
C15H12N2O3
分子量
268.27
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
TMBIM6 antagonist-1 是一个有潜力的 TMBIM6 拮抗剂,抑制 TMBIM6 与 mTORC2 结合,降低 mTORC2 活性,调节TMBIM6 释放 Ca2+
生物活性
TMBIM6 antagonist-1, a potential TMBIM6 antagonist, prevents TMBIM6 binding to mTORC2, decreases mTORC2 activity, and also regulates TMBIM6-leaky Ca.
性状
Solid
体外研究(In Vitro)
TMBIM6 antagonist-1 (BIA, 0.5-10 μM, 3 days) significantly and dose-dependently inhibits cell viability in HT1080, MCF7, MDA-MB-2341 and SKBR3 cells, with IC50 values of 1.7?±?0.1?μM for HT1080, 2.6?±?0.4?μM for MCF cells, 2.6?±?0.5?μM for MDA-MB-231 cells, and 2.4?±?0.4?μM for SKBR3 cells, respectively.
TMBIM6 antagonist-1 (BIA, 10 μM) treatment decreases cell migration in HT1080, MCF7, MDA-MB-231, and SKBR3 cells, not TMBIM6 KO HT1080 cells.
has not independently confirmed the accuracy of these methods. They are for reference only.
TMBIM6 antagonist-1 (1?mg/kg, IP 5 days per week during 25 days) significantly impaires cell-driven tumor growth.
has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Hyun-Kyoung Kim, et al. TMBIM6/BI-1 contributes to cancer progression through assembly with mTORC2 and AKT activation. Nat Commun. 2020 Aug 11;11(1):4012.
溶解度数据
In Vitro: DMSO : 50 mg/mL (186.38 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。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。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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