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S81857

SENKTIDE

源葉(MedMol) ≥98%
  • 英文名:
  • SUCCINYL-ASP-PHE-ME-PHE-GLY-LEU-MET-NH2
  • 別名:
  • [SUCCINYL-ASP6,ME-PHE8] SUBSTANCE P;SUCCINYL-(ASP6,N-ME-PHE8)-SUBSTANCE P (6-11);[SUCCINYL-ASP6 N-ME-PHE8]-SUBSTANCE P (6-11) (SENKTIDE);[SUCCINYL-ASP6,N-ME-PHE8]-SUBSTANCE P, FRAGMENT 6-11;SUCCINYL-
  • CAS號(hào):
  • 106128-89-6
  • 分子式:
  • C40H55N7O11S
  • 分子量:
  • 841.97
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 數(shù)量計(jì)量單位 加入購(gòu)物車(chē)...
源葉(MedMol) S81857-500ug ≥98% ¥427.00元 10 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S81857-1mg ≥98% ¥570.00元 10 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S81857-5mg ≥98% ¥1320.00元 10 - - - EA 加入購(gòu)物車(chē)
源葉(MedMol) S81857-10mg ≥98% ¥1990.00元 4 - - - EA 加入購(gòu)物車(chē)
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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

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  • 提示:詳情請(qǐng)下載說(shuō)明書(shū)。
  • 產(chǎn)品描述: Senktide is a tachykinin NK3 receptor agonist.
  • 靶點(diǎn): NK3 receptor;Neurokininreceptor
  • 體內(nèi)研究:
    I.c.v. injection of Senktide causes a dose-dependent increase in total distance traveled (F6,72=6.344, P<0.001). This increase reaches statistical significance compare to the vehicle-treated group at 0.06 nmol and higher. The Senktide-induced increase in locomotor activity brought about by 0.1 nmol of Senktide is significantly and dose-dependently decreased by the tachykinin NK3 receptor antagonists talnetant at 30 mg/kg and SB222200 at 30 mg/kg, but not by osanetant, when tested in parallel in a single experiment (F7,78=10.32, P<0.001), although a non-significant reduction is observed. However, when tested using another vehicle (Vitamin E and glycofurol), osanetant does decrease activity significantly compare to Senktide-treated gerbils (F2,30=10.10, P<0.001)
  • 參考文獻(xiàn):
    1. Nordquist RE, et al. The tachykinin NK3 receptor agonist senktide induces locomotor activity in male Mongolian gerbils. Eur J Pharmacol. 2008 Dec 14;600(1-3):87-92. 2. Keegan KD, et al. The selective NK3 receptor agonist senktide excites a subpopulation of dopamine-sensitiveneurones in the rat substantia nigra pars compacta in vitro. Br J Pharmacol. 1992 Jan;105(1):3-5.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 1.188 ml 5.938 ml 11.877 ml
    5 mM 0.238 ml 1.188 ml 2.375 ml
    10 mM 0.119 ml 0.594 ml 1.188 ml
    50 mM 0.024 ml 0.119 ml 0.238 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(hù)參考交流研究之用。
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質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)


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