TMBIM6 antagonist-1,99.80%

产品编号:Bellancom-137175| CAS NO:123134-61-2| 分子式:C15H12N2O3| 分子量:268.27

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-137175
2500.00 杭州 北京(现货)
Bellancom-137175
4000.00 杭州 北京(现货)
Bellancom-137175
11500.00 杭州 北京(现货)
Bellancom-137175
0.00 杭州 北京(现货)

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TMBIM6 antagonist-1

产品介绍 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 Ca2+.

体外研究

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.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: HT1080, MCF7, MDA-MB-2341 and SKBR3 cells.
Concentration: 0.5-10 μM.
Incubation Time: 3 days.
Result: Inhibited cell viability.

Western Blot Analysis

Cell Line: WT and TMBIM6 KO HT1080 cells.
Concentration: 0, 2, 5 μM.
Incubation Time:
Result: Downregulated the protein levels of AKT-pS473.
体内研究
(In Vivo)

TMBIM6 antagonist-1 (1 mg/kg, IP 5 days per week during 25 days) significantly impaires cell-driven tumor growth.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Six- to eight-week BklNbt:BALB/c/nu/nu old mice (HT1080 and MDA-MB-231 cells).
Dosage: 1 mg/kg.
Administration: IP 5 days per week during 25 days.
Result: Impaired cell-driven tumor growth.
体内研究

TMBIM6 antagonist-1 (1 mg/kg, IP 5 days per week during 25 days) significantly impaires cell-driven tumor growth.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Six- to eight-week BklNbt:BALB/c/nu/nu old mice (HT1080 and MDA-MB-231 cells).
Dosage: 1 mg/kg.
Administration: IP 5 days per week during 25 days.
Result: Impaired cell-driven tumor growth.
体内研究

TMBIM6 antagonist-1 (1 mg/kg, IP 5 days per week during 25 days) significantly impaires cell-driven tumor growth.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Six- to eight-week BklNbt:BALB/c/nu/nu old mice (HT1080 and MDA-MB-231 cells).
Dosage: 1 mg/kg.
Administration: IP 5 days per week during 25 days.
Result: Impaired cell-driven tumor growth.
性状Solid
溶解性数据
In Vitro: 

DMSO : 50 mg/mL (186.38 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 3.7276 mL 18.6379 mL 37.2759 mL
5 mM 0.7455 mL 3.7276 mL 7.4552 mL
10 mM 0.3728 mL 1.8638 mL 3.7276 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

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
In solvent -80°C 6 months
-20°C 1 month
参考文献

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