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APS-2-79 (hydrochloride)

    98%

APS-2-79 (hydrochloride)

源葉(MedMol)
S81424
2002381-31-7
C23H22ClN3O3
423.89208
品牌 貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 購(gòu)買(mǎi)數(shù)量
源葉(MedMol) S81424-5mg 98% ¥480.00元 9 - - -
源葉(MedMol) S81424-10mg 98% ¥888.00元 10 - - -
源葉(MedMol) S81424-25mg 98% ¥2000.00元 10 - - -
源葉(MedMol) S81424-50mg 98% ¥3600.00元 >10 - - -
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

APS-2-79 hydrochloride is a KSR-dependent MEK antagonist. APS-2-79 inhibits ATPbiotin binding to KSR2 within the KSR2-MEK1 complexe with an IC50 of 120 nM. APS-2-79 makes the stabilization of the KSR inactive state antagonizes oncogenic Ras-MAPK signaling
產(chǎn)品描述: APS-2-79 hydrochloride is a KSR-dependent MEK antagonist. APS-2-79 inhibits ATPbiotin binding to KSR2 within the KSR2-MEK1 complexe with an IC50 of 120 nM. APS-2-79 makes the stabilization of the KSR inactive state antagonizes oncogenic Ras-MAPK signaling
靶點(diǎn): KSR2:120 nM (IC50);MEK1;MEK;?MAPK
體外研究: APS-2-79 (5 μM) suppresses KSR-stimulated MEK and ERK phosphorylation in 293H cells. APS-2-79 (1 μM) enhances the efficacy of the clinical MEK inhibitor trametinib within cancer cell lines containing K-Ras mutations
參考文獻(xiàn): 1. Dhawan NS, et al. Small molecule stabilization of the KSR inactive state antagonizes oncogenic Ras signalling. Nature. 2016 Sep 1;537(7618):112-116.
溶解性: DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.359 ml 11.795 ml 23.591 ml
5 mM 0.472 ml 2.359 ml 4.718 ml
10 mM 0.236 ml 1.18 ml 2.359 ml
50 mM 0.047 ml 0.236 ml 0.472 ml
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參考文獻(xiàn)

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