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S84821

Ro 67-7476

源葉(MedMol) 98%
  • 英文名:
  • Ro 67-7476
  • 別名:
  • Pyrrolidine,2-(4-fluorophenyl)-1-[(4-methylphenyl)sulfonyl]-,(2S)
  • CAS號:
  • 298690-60-5
  • 分子式:
  • C17H18FNO2S
  • 分子量:
  • 319.3937
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S84821-5mg 98% ¥1000.00元 預計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S84821-10mg 98% ¥1600.00元 預計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S84821-50mg 98% ¥6000.00元 預計交期:2-3天 - - - EA 加入購物車
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參考文獻

質(zhì)檢證書(COA)

摩爾濃度計算器

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  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Ro 67-7476 is a potent positive allosteric modulator of mGluR1 and potentiates glutamate-induced calcium release in HEK293 cells expressing rat mGluR1a with an EC50 of 60.1 nM. Ro 67-7476 is a potent P-ERK1/2 agonist and activates ERK1/2 phosphorylation in the absence of exogenously added glutamate (EC50=163.3 nM)
  • 靶點: mGluR1a:60.1 nM (EC50);GluR
  • 體外研究:
    In the Purkinje cells of rat cerebellar slices, Ro 67-7476 increases the amplitude of mGluR1 excitatory postsynaptic potentials (EPSCs) evoked by 2,3-dihydroxy-6-nitro-7-sulfamoylbenzoquionxaline, picrotoxin, or AP5. Ro 67-7476 activates ERK1/2 phosphorylation in the absence of exogenously added glutamate (EC50=163.3 nM). The EC50 value of full P-ERK1/2 activation for Ro 67-7476 are nearly identical to the EC50 for calcium mobilization potentiation. Ro 67-7476 increases basal cAMP production approximately by 8%. It potentiated threshold responses to glutamate in the cAMP accumulation assay, with an EC50 value of 17.7 μM
  • 參考文獻:
    1. F Knoflach, et al. Positive allosteric modulators of metabotropic glutamate 1 receptor: characterization, mechanism of action, and binding site. Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13402-7 2. Kamondanai Hemstapat, et al. A novel class of positive allosteric modulators of metabotropic glutamate receptor subtype 1 interact with a site distinct from that of negative allosteric modulators. Mol Pharmacol. 2006 Aug;70(2):616-26. 3. Douglas J Sheffler, et al. Allosteric potentiators of metabotropic glutamate receptor subtype 1a differentially modulate independent signaling pathways in baby hamster kidney cells. Neuropharmacology. 2008 Sep;55(4):419-27
  • 溶解性: Soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 3.131 ml 15.655 ml 31.309 ml
    5 mM 0.626 ml 3.131 ml 6.262 ml
    10 mM 0.313 ml 1.565 ml 3.131 ml
    50 mM 0.063 ml 0.313 ml 0.626 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。
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本計算器可幫助您計算出特定溶液中溶質(zhì)的質(zhì)量、溶液濃度和體積之間的關系,公式為:


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


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