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STO-609

    98%

7-Oxo-7H-benzimidazo[2,1-a]benz[de]isoquinoline-3-carboxylic Acid

源葉(MedMol)
S80770
52029-86-4
C19H10N2O3
314.29
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S80770-1mg 98% ¥42.00元 2 - - -
源葉(MedMol) S80770-5mg 98% ¥135.00元 2 - - -
源葉(MedMol) S80770-10mg 98% ¥225.00元 5 - - -
源葉(MedMol) S80770-25mg 98% ¥460.00元 7 - - -
源葉(MedMol) S80770-50mg 98% ¥800.00元 3 - - -
源葉(MedMol) S80770-100mg 98% ¥1130.00元 預計交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(2篇) 質檢證書(COA) 摩爾濃度計算器 相關產(chǎn)品

產(chǎn)品介紹

STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. STO-609 inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.
產(chǎn)品描述: STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. STO-609 inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.
靶點: Ki: 80 ng/mL (CaM-KKα), 15 ng/mL (CaM-KKβ);CaMK;AMPK;Autophagy
參考文獻: 1. Tokumitsu H, et al. STO-609, a specific inhibitor of the Ca(2+)/calmodulin-dependent protein kinase kinase. J Biol Chem. 2002 May 3;277(18):15813-8. 2. Kukimoto-Niino M, et al. Crystal structure of the Ca2+/calmodulin-dependent protein kinase kinase in complex with the inhibitor STO-609. J Biol Chem. 2011 Jun 24;286(25):22570-9.
溶解性: DMSO  :  6.25  mg/mL  (19.89  mM;  ultrasonic  and  warming  and  heat  to  80°C)    DMF  :  5.56  mg/mL  (17.69  mM;  Need  ultrasonic)    H2O  :  <  0.1  mg/mL  (insoluble)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.182 ml 15.909 ml 31.818 ml
5 mM 0.636 ml 3.182 ml 6.364 ml
10 mM 0.318 ml 1.591 ml 3.182 ml
50 mM 0.064 ml 0.318 ml 0.636 ml
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摩爾濃度計算器

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