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PI3K/Akt/mTOR-IN-2
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
PI3K/Akt/mTOR-IN-2图片
CAS NO:2757804-89-8
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品介绍
PI3K/Akt/mTOR-IN-2 是一种有效的PI3K/AKT/mTOR抑制剂。PI3K/Akt/mTOR-IN-2 具有抗癌作用,并对 MDA-MB-231 细胞具有选择性,IC50为 2.29 μM。PI3K/Akt/mTOR-IN-2 可诱导癌细胞周期阻滞和细胞凋亡 (apoptosis)。
生物活性

PI3K/Akt/mTOR-IN-2 is aPI3K/AKT/mTORpathway inhibitor. PI3K/Akt/mTOR-IN-2 possess anti-cancer effects and selectivity against MDA-MB-231 cells withIC50value of 2.29 μM. PI3K/Akt/mTOR-IN-2 can inducecancercell cycle arrest andapoptosis[1].

IC50& Target

IC50: 2.29 μM (PI3K/AKT/mTOR) in MDA-MB-231[1]

体外研究
(In Vitro)

PI3K/Akt/mTOR-IN-2 (compound 23) (0.5 - 100 μM; 72 hours) exhibits effective anti-cancer activity with IC50s of 2.29 - 24.63 μM, of which, IC50in MDA-MB-231 is 2.29 μM[1].
PI3K/Akt/mTOR-IN-2 (1 μM, 2 μM and 4 μM; 24 hours) induces growth inhibition of MDA-MB-231 cells by cell cycle arrest at G0/G1[1].
PI3K/Akt/mTOR-IN-2 (1 μM, 2 μM and 4 μM; 24, 48 and 72 hours) induces apoptosis in MDA-MB-231 cells with both dose- and time-dependent manners[1].
PI3K/Akt/mTOR-IN-2 (1 μM, 2 μM and 4 μM; 48 hours) increases the expression of Bax, and decreases the expression of Bcl-2 in MDA-MB-231 cells[1].
PI3K/Akt/mTOR-IN-2 (1 μM, 2 μM and 4 μM; 24 hours) induces mitochondria-dependent apoptosis in MDA-MB-231 cells through disruption of MMP, accumulation of ROS, depletion of GSH and elevation of intracellular Ca2+[1].

Cell Proliferation Assay

Cell Line:PC3, BGC-823, A549, MCF-7, MDA-MB-231 cells and MCF-10A cells[1]
Concentration:0.5 - 100 μM
Incubation Time:72 hours
Result:Exhibited effective anti-cancer activity with IC50s of 2.29 - 24.63 μM, of which, IC50in MDA-MB-231 was 2.29 μM.

Cell Cycle Analysis

Cell Line:MDA-MB-231[1]
Concentration:1 μM, 2 μM and 4 μM
Incubation Time:24 hours
Result:Induced growth inhibition of MDA-MB-231 cells by cell cycle arrest at G0/G1.

Apoptosis Analysis

Cell Line:MDA-MB-231[1]
Concentration:1 μM, 2 μM and 4 μM
Incubation Time:24, 48 and 72 hours
Result:Induced apoptosis in MDA-MB-231 cells with both dose- and time-dependent manners.

Western Blot Analysis

Cell Line:MDA-MB-231[1]
Concentration:1 μM, 2 μM and 4 μM
Incubation Time:48 hours
Result:Increased the expression of Bax, and decreased the expression of Bcl-2
分子量

285.29

性状

Solid

Formula

C17H13F2NO

CAS 号

2757804-89-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : ≥ 100 mg/mL(350.52 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.5052 mL17.5260 mL35.0521 mL
5 mM0.7010 mL3.5052 mL7.0104 mL
10 mM0.3505 mL1.7526 mL3.5052 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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。