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S80272

Win 55,212-2 Mesylate

源葉(MedMol) 98%
  • 英文名:
  • Win 55,212-2 Mesylate
  • 別名:
  • (R)-(+)-WIN 55,212-2 甲磺酸鹽;(R)-(5-Methyl-3-(morpholinoMethyl)-2,3-Dihydro-[1,4]Oxazino[2,3,4-hi]Indol-6-yl)(Naphthalen-1-yl)Methanone Methanesulfonate
  • CAS號:
  • 131543-23-2
  • 分子式:
  • C28H30N2O6S
  • 分子量:
  • 522.61
  • 核磁/質(zhì)譜:
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) S80272-5mg 98% ¥240.00元 預(yù)計交期:2-3天 0 0 0 EA 加入購物車
源葉(MedMol) S80272-10mg 98% ¥392.00元 預(yù)計交期:2-3天 0 0 0 EA 加入購物車
源葉(MedMol) S80272-25mg 98% ¥880.00元 預(yù)計交期:2-3天 0 0 0 EA 加入購物車
源葉(MedMol) S80272-50mg 98% ¥1600.00元 預(yù)計交期:2-3天 0 0 0 EA 加入購物車
源葉(MedMol) S80272-100mg 98% ¥2800.00元 預(yù)計交期:2-3天 0 0 0 EA 加入購物車
源葉(MedMol) S80272-200mg 98% ¥4960.00元 預(yù)計交期:2-3天 0 0 0 EA 加入購物車
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產(chǎn)品介紹

參考文獻

質(zhì)檢證書(COA)

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  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: WIN 55,212-2 Mesylate is a potent aminoalkylindole cannabinoid (CB) receptor agonist with Kis of 62.3 and 3.3 nM for human recombinant CB1 and CB2 receptors, respectively.
  • 靶點: Ki: 62.3 nM (human recombinant CB1), 3.3 nM (human recombinant CB2)
  • 體內(nèi)研究:
    In the prefrontal cortex WIN 55,212-2 (0.1 and 1 mg/kg i.p.) increases dialysate glutamate levels from of the awake rat, while the lower (0.01 mg/kg) and the higher (2 mg/kg) doses are ineffective. Furthermore, the WIN 55,212-2 (0.1 mg/kg)- induced increase of dialysate glutamate levels is counteracted by pretreatment with the selective CB(1) receptor antagonist SR141716A (0.1 mg/kg, i.p.) and by the local perfusion with a low-calcium Ringer solution (Ca2+ 0.2 mM). WIN 55,212-2 (0.5, 1, 3, 5, 10 and 15 mg/kg, i.p.) does not alter the seizure threshold at low doses, while higher doses of the drug significantly increases the threshold in a dose-dependent manner. The anticonvulsant effect of WIN 55,212-2, which is observed with doses as high as 5 mg/kg, can be observed with doses as low as 0.5 mg/kg in groups pre-treated with 20 mg/kg of pioglitazone
  • 參考文獻:
    1. Felder CC, et al. Comparison of the pharmacology and signal transduction of the human cannabinoid CB1 and CB2 receptors. Mol Pharmacol. 1995 Sep;48(3):443-50. 2. Ferraro L, et al. The cannabinoid receptor agonist WIN 55,212-2 regulates glutamate transmission in rat cerebral cortex: an in vivo and in vitro study. Cereb Cortex. 2001 Aug;11(8):728-33. 3. Price TJ, et al. Cannabinoid receptor-independent actions of the aminoalkylindole WIN 55,212-2 on trigeminal sensory neurons. Br J Pharmacol. 2004 May;142(2):257-66. 4. Payandemehr B, et al. Involvement of PPAR receptors in the anticonvulsant effects of a cannabinoid agonist, WIN 55,212-2. Prog Neuropsychopharmacol Biol Psychiatry. 2015 Mar 3;57:140-5
  • 溶解性: DMSO  :  200  mg/mL  (382.69  mM;  Need  ultrasonic)
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.913 ml 9.567 ml 19.135 ml
    5 mM 0.383 ml 1.913 ml 3.827 ml
    10 mM 0.191 ml 0.957 ml 1.913 ml
    50 mM 0.038 ml 0.191 ml 0.383 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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