| 货号 | 规格 | 价格 | 上海 | 北京 | 珠海 | 重庆 | 武汉 | 购买数量 |
|---|---|---|---|---|---|---|---|---|
S80622-5mg买3赠1 |
99.70% | ￥160.00 |
2 | - | - | - | - |
|
S80622-10mg买3赠1 |
99.70% | ￥208.00 |
4 | - | - | - | - |
|
S80622-25mg买3赠1 |
99.70% | ￥248.00 |
7 | - | - | - | - |
|
S80622-50mg买3赠1 |
99.70% | ￥408.00 |
5 | - | - | - | - |
|
S80622-100mg买3赠1 |
99.70% | ￥720.00 |
4 | - | - | - | - |
|
S80622-200mg买3赠1 |
≥99% | ￥1280.00 |
货期：2-3天 | - | - | - | - |
|
| 产品描述： | T0070907 is a potent PPARγ antagonist with a Ki of 1 nM. | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 靶点： | PPARγ:1 nM (Ki);PPARδ:1.8 μM (Ki);PPARα:0.85 μM (Ki);PPAR | ||||||||||||||||||||
| 参考文献： | 1. An Z, et al. T0070907 inhibits repair of radiation-induced DNA damage by targeting RAD51. Toxicol In Vitro. 2016 Dec;37:1-8 2. An Z, et al. T0070907, a PPAR γ inhibitor, induced G2/M arrest enhances the effect of radiation in human cervical cancer cells through mitotic catastrophe. Reprod Sci. 2014 Nov;21(11):1352-61. 3. Kawahara A, et al. Peroxisome proliferator-activated receptor γ (PPARγ)-independent specific cytotoxicity against immature adipocytes induced by PPARγ antagonist T0070907. Biol Pharm Bull. 2013;36(9):1428-34 4. Lee G, et al. T0070907, a selective ligand for peroxisome proliferator-activated receptor gamma, functions as an antagonist of biochemical and cellular activities. J Biol Chem. 2002 May 31;277(22):19649-57. Epub 2002 Mar 4 | ||||||||||||||||||||
| 溶解性： | DMSO : 62.5 mg/mL (225.10 mM; ultrasonic and warming and heat to 60°C) H2O : 1.1 mg/mL (3.96 mM; Need ultrasonic) | ||||||||||||||||||||
| 保存条件： | -20℃ | ||||||||||||||||||||
| 配置溶液浓度参考： |
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| 注意： | 部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
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