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GSK180736A

    
98%

GSK180736A

源葉(MedMol)
S81535 一鍵復(fù)制產(chǎn)品信息
817194-38-0
C19H16FN5O2
365.3611
貨號 規(guī)格 價(jià)格 上海 北京 武漢 南京 購買數(shù)量
S81535-1mg 98% ¥229.50 10 - - -
S81535-5mg 98% ¥527.00 6 - - -
S81535-10mg 98% ¥722.50 6 - - -
S81535-25mg 98% ¥1530.00 6 - - -
S81535-50mg 98% ¥2890.00 5 - - -
S81535-100mg 98% ¥3800.00 貨期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

GSK180736A is potent Rho-associated coiled-coil kinase 1 (ROCK1) inhibitor with an IC50 of 100 nM. GSK180736A is also a selective and ATP-competitive G protein-coupled receptor kinase 2 (GRK2) inhibitor with an IC50 of 0.77 μM

產(chǎn)品描述: GSK180736A is potent Rho-associated coiled-coil kinase 1 (ROCK1) inhibitor with an IC50 of 100 nM. GSK180736A is also a selective and ATP-competitive G protein-coupled receptor kinase 2 (GRK2) inhibitor with an IC50 of 0.77 μM
靶點(diǎn): ROCK1:100 nM (IC50);GRK2:770 nM (IC50);ROCK;?GRK;?PKA
體外研究: GSK180736A is a compound structurally similar to paroxetine that is developed as a ROCK inhibitor, is shown to be an even more potent and selective inhibitor of GRK2 with an IC50 of 0.77 μM and more than 100-fold selectivity over other GRKs. ROCK1 is a potential therapeutic target in the treatment of cardiovascular diseases such as hypertension. GSK180736A is a weak inhibitor of PKA with an IC50 of 30 μM, but highly potent against ROCK1 (IC50=100 nM)
參考文獻(xiàn): 1. Waldschmidt HV, et al. Structure-Based Design, Synthesis, and Biological Evaluation of Highly Selective and Potent G Protein-Coupled Receptor Kinase 2 Inhibitors. J Med Chem. 2016 Apr 28;59(8):3793-807.
溶解性: soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.737 ml 13.685 ml 27.37 ml
5 mM 0.547 ml 2.737 ml 5.474 ml
10 mM 0.274 ml 1.369 ml 2.737 ml
50 mM 0.055 ml 0.274 ml 0.547 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(xiàn)

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