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CP-466722

    
98%

CP-466722

源葉(MedMol)
S80075 一鍵復(fù)制產(chǎn)品信息
1080622-86-1
C17H15N7O2
349.35
CP466722;1-(6,7-二甲氧基-4-喹唑啉基)-3-(2-吡啶基)-1H-1,2,4-三唑-5-胺
貨號(hào) 規(guī)格 價(jià)格 上海 北京 武漢 南京 購(gòu)買(mǎi)數(shù)量
S80075-1mg 98% ¥60.00 6 - - -
S80075-2mg 98% ¥80.00 7 - - -
S80075-5mg 98% ¥140.00 7 - - -
S80075-10mg 98% ¥240.00 8 - - -
S80075-25mg 98% ¥480.00 5 - - -
S80075-50mg 98% ¥680.00 貨期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(shū)(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

CP-466722 is a rapidly reversible inhibitor of ATM, with an IC50 of 4.1 μM, and has no effects on PI3K or closely related PI3K-like protein kinase (PIKK) family members.

產(chǎn)品描述: CP-466722 is a rapidly reversible inhibitor of ATM, with an IC50 of 4.1 μM, and has no effects on PI3K or closely related PI3K-like protein kinase (PIKK) family members.
靶點(diǎn): ATM:4.1 μM (IC50);ATM/ATR
參考文獻(xiàn): 1. Rainey MD, et al. Transient inhibition of ATM kinase is sufficient to enhance cellular sensitivity to ionizing radiation. Cancer Res. 2008 Sep 15;68(18):7466-74. 2. Guo K, et al. Development of a cell-based, high-throughput screening assay for ATM kinase inhibitors. J Biomol Screen. 2014 Apr;19(4):538-46. 3. W?sierska-G?dek J, et al. Interactions Between Ataxia Telangiectasia Mutated Kinase Inhibition, Poly(ADP-ribose) Polymerase-1 Inhibition and BRCA1 Status in Breast Cancer Cells. J Cancer Prev. 2014 Jun;19(2):125-36.
溶解性: DMSO  :  1  mg/mL  (2.86  mM;  Need  ultrasonic)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.862 ml 14.312 ml 28.625 ml
5 mM 0.572 ml 2.862 ml 5.725 ml
10 mM 0.286 ml 1.431 ml 2.862 ml
50 mM 0.057 ml 0.286 ml 0.572 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(hù)參考交流研究之用。

參考文獻(xiàn)

質(zhì)檢證書(shū)(COA)

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批號(hào):JS298415 貨號(hào):S20001-25g
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摩爾濃度計(jì)算器

質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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