CAS NO: | 97322-87-7 |
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 |
500mg | 电议 |
生物活性 | Troglitazone is aPPARγagonist, withEC50s of 550 nM and 780 nM for human and murine PPARγ receptor, respectively. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | Troglitazone is aPPARγagonist, with EC50s of 550 nM and 780 nM for human and murine PPARγ receptor, respectively[1]. Troglitazone (2-200 μM) is cytotoxic to the pancreatic cancer cell lines (MIA Paca2 and PANC-1 cells), with IC50s of 49.9 ± 1.2 and 51.3 ± 5.3 μM, respectively. Troglitazone (50 μM) increases chromatin condensation in MIA Paca2 and PANC-1 cells, enhances the activity of caspase-3 and decreases Bcl-2 expression[2]. Troglitazone (0, 1, 2, and 4 μM) sensitizes TRAIL-mediated apoptosis in human lung adenocarcinoma cells. Troglitazone enhancement of TRAIL-induced apoptosis is blocked by inhibition of autophagy, via activation of autophagy flux. In addition, the effects of troglitazone are induced by PPARγ activation in A549 cells[3]. | ||||||||||||||||
体内研究 (In Vivo) | Troglitazone (200 mg/kg, p.o.) shows inhibitory effects on the growth of tumor in the MIA Paca2 xenograft model[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 441.54 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H27NO5S | ||||||||||||||||
CAS 号 | 97322-87-7 | ||||||||||||||||
中文名称 | 曲格列酮;特洛格列酮 | ||||||||||||||||
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 : 160 mg/mL(362.37 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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