S80622 |
T0070907 |
源葉(MedMol) | 99% |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.602 ml | 18.008 ml | 36.015 ml |
5 mM | 0.72 ml | 3.602 ml | 7.203 ml |
10 mM | 0.36 ml | 1.801 ml | 3.602 ml |
50 mM | 0.072 ml | 0.36 ml | 0.72 ml |
- 提示:詳情請下載說明書。
- 產(chǎn)品描述: T0070907 is a potent PPARγ antagonist with a Ki of 1 nM.
- 靶點: PPARγ:1 nM (Ki);PPARδ:1.8 μM (Ki);PPARα:0.85 μM (Ki);PPAR
- 參考文獻(xiàn):
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)
- 保存條件: -20℃
- 配置溶液濃度參考:
1mg 5mg 10mg 1 mM 3.602 ml 18.008 ml 36.015 ml 5 mM 0.72 ml 3.602 ml 7.203 ml 10 mM 0.36 ml 1.801 ml 3.602 ml 50 mM 0.072 ml 0.36 ml 0.72 ml
- 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
輸入產(chǎn)品批號:
本計算器可幫助您計算出特定溶液中溶質(zhì)的質(zhì)量、溶液濃度和體積之間的關(guān)系,公式為:
質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)