S80816 |
KU-55933 (ATM Kinase Inhibitor) |
源葉(MedMol) | 99% |
- 提示:詳情請下載說明書。
- 產(chǎn)品描述: KU-55933 is a potent ATM inhibitor with an IC50 and Ki of 12.9 and 2.2 nM, respectively, and is highly selective for ATM as compared to DNA-PK, PI3K/PI4K, ATR and mTOR.
- 靶點(diǎn): ATM:12.9 nM (IC50);DNA-PK:2500 nM (IC50);mTOR:9300 nM (IC50);PI3K:16600 nM (IC50)
- 參考文獻(xiàn):
1. Hickson I, et al. Identification and characterization of a novel and specific inhibitor of the ataxia-telangiectasia mutated kinase ATM. Cancer Res. 2004 Dec 15;64(24):9152-9 2. Khalil HS, et al. Pharmacological inhibition of ATM by KU55933 stimulates ATM transcription.Exp Biol Med (Maywood). 2012 Jun;237(6):622-34. Epub 2012 Jun 22. 3. Kim YD, et al. Orphan nuclear receptor SHP negatively regulates growth hormone-mediated induction of hepatic gluconeogenesis through inhibition of STAT5 transactivation.J Biol Chem. 2012 Sep 12.
- 溶解性: DMSO : 80 mg/mL (202.28 mM; Need ultrasonic)
- 保存條件: -20℃
- 配置溶液濃度參考:
1mg 5mg 10mg 1 mM 2.529 ml 12.643 ml 25.285 ml 5 mM 0.506 ml 2.529 ml 5.057 ml 10 mM 0.253 ml 1.264 ml 2.529 ml 50 mM 0.051 ml 0.253 ml 0.506 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。
- 1. 梁燕 賈珍 陳仲海 阿良德.七氟烷對大鼠肺缺血再灌注損傷中ATM的影響[J].中國老年學(xué)雜志 2018 38(15):3756-3759.
輸入產(chǎn)品批號:
本計(jì)算器可幫助您計(jì)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)