Pimasertib (AS-703026)

    
96%

Pimasertib (AS-703026)

源葉(MedMol)
S80212 一鍵復制產(chǎn)品信息
1236699-92-5
C15H15FIN3O3
431.2
MSC1936369B;(S)-N-(2,3-dihydroxypropyl)-3-(2-fluoro-4-iodophenylamino)isonicotinamide
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S80212-2mg 96% ¥140.00 5 - - -
S80212-5mg 96% ¥290.00 6 - - -
S80212-10mg 96% ¥470.00 6 - - -
S80212-25mg 96% ¥800.00 6 - - -
S80212-50mg 96% ¥1400.00 5 - - -
S80212-100mg 96% ¥2350.00 貨期:2-3天 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關產(chǎn)品

產(chǎn)品介紹

Pimasertib (AS703026) is a highly selective, ATP non-competitive allosteric orally available MEK1/2 inhibitor

產(chǎn)品描述: Pimasertib (AS703026) is a highly selective, ATP non-competitive allosteric orally available MEK1/2 inhibitor
靶點: MEK1;MEK2;MEK
體內(nèi)研究: Pimasertib (15, 30 mg/kg) significantly inhibits the growth of tumor in the human H929 MM xenograft model in CB17 SCID mice. Pimasertib (10 mg/kg, p.o.) inhibits tumor growth of cetuximab-resistant tumor attributed by K-ras mutation
參考文獻: 1. Kim K, et al. Blockade of the MEK/ERK signalling cascade by AS703026, a novel selective MEK1/2 inhibitor, induces pleiotropic anti-myeloma activity in vitro and in vivo. Br J Haematol, 2010, 149(4), 537-549. 2. Park SJ, et al. The MEK1/2 inhibitor AS703026 circumvents resistance to the BRAF inhibitor PLX4032 in human malignant melanoma cells. Am J Med Sci. 2013 Dec;346(6):494-8. 3. Yoon J, et al. MEK1/2 inhibitors AS703026 and AZD6244 may be potential therapies for KRAS mutated colorectal cancer that is resistant to EGFR monoclonal antibody therapy. Cancer Res, 2011, 71(2), 445-453.
溶解性: DMSO  :  ≥  100  mg/mL  (231.91  mM)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.319 ml 11.596 ml 23.191 ml
5 mM 0.464 ml 2.319 ml 4.638 ml
10 mM 0.232 ml 1.16 ml 2.319 ml
50 mM 0.046 ml 0.232 ml 0.464 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。

參考文獻

質(zhì)檢證書(COA)

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摩爾濃度計算器

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