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S86590

Cabergoline

源葉(MedMol) 99%
  • 英文名:
  • Cabergoline
  • 別名:
  • 卡麥角林
  • CAS號(hào):
  • 81409-90-7
  • 分子式:
  • C26H37N5O2
  • 分子量:
  • 451.6
  • 核磁/質(zhì)譜:
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...
源葉(MedMol) S86590-5mg 99% ¥425.00元 3 - - - EA 加入購(gòu)物車
源葉(MedMol) S86590-10mg 99% ¥637.50元 8 - - - EA 加入購(gòu)物車
源葉(MedMol) S86590-50mg 99% ¥2550.00元 7 - - - EA 加入購(gòu)物車
源葉(MedMol) S86590-100mg 99% ¥4300.00元 5 - - - EA 加入購(gòu)物車
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產(chǎn)品介紹

參考文獻(xiàn)

質(zhì)檢證書(shū)(COA)

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  • 提示:詳情請(qǐng)下載說(shuō)明書(shū)。
  • 產(chǎn)品描述: Cabergoline is an ergot derived-dopamine D2-like receptor agonist that has high affinity for?D2,?D3, and?5-HT2B?receptors (Ki=0.7, 1.5, and 1.2, respectively).
  • 靶點(diǎn): D3 Receptor;D2 Receptor;DopamineReceptor;5-HTReceptor;Autophagy
  • 體內(nèi)研究:
    Cabergoline has a longer elimination half-life (63 to 109 h) compared with other D2-like receptor agonists, both a long-lasting clinical effect following single-dose administration, and an improvement in the quality of life of patients with chronic diseases are expected. The most significant reduction in rapid eye movement (REM) sleep bout number occurred during the light phase, in which Cabergoline-injected female handled mice has 67.3% less REM sleep bouts (F(1,11)=12.892, P=0.004) than Cabergoline-injected females that are restrained, although the greatest number in reduction of REM sleep bouts occurr during the dark phase (82.3% fewer REM sleep bouts; F(1,11)=3.667, P=0.082). In male mice, Cabergoline reduces baseline Prolactin (PRL) levels (98.5%; F(1,6)=13.192, P=0.011) from 5.8±1.3 to 0.08 ng/mL within 2 hours of injection. After a 7-day recovery period, PRL levels return to values that are not different from baseline (5.0±0.60 ng/mL; F(1,6)=0.715, P=0.43).
  • 參考文獻(xiàn):
    1. Odaka H, et al. Cabergoline, dopamine D2 receptor agonist, prevents neuronal cell death under oxidative stress via reducing excitotoxicity. PLoS One. 2014 Jun 10;9(6):e99271. 2. Jefferson F, et al. A dopamine receptor d2-type agonist attenuates the ability of stress to alter sleep in mice. Endocrinology. 2014 Nov;155(11):4411-21.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.214 ml 11.072 ml 22.143 ml
    5 mM 0.443 ml 2.214 ml 4.429 ml
    10 mM 0.221 ml 1.107 ml 2.214 ml
    50 mM 0.044 ml 0.221 ml 0.443 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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