CLP2025 Biotin-Neurokinin B 神经肽及相关肽 1926163-17-8

CLP2025 Biotin-Neurokinin B 神经

肽及相关肽 1926163-17-8
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  • ¥990 - 3470
  • Solarbio|ActivAb
  • 北京
  • CLP2025
  • 2025年07月30日
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    • 详细信息
    • 技术资料
    • 保存条件

      Store at -20℃,2 years.(Avoid freeze/thaw cycles)

    • 保质期

      Store at -20℃,2 years.(Avoid freeze/thaw cycles)

    • 英文名

      Biotin-Neurokinin B

    • 库存

      现询

    • 供应商

      北京索莱宝科技有限公司

    • 规格

      10mg/5mg/1mg

    规格:10mg产品价格:¥3470.0
    规格:5mg产品价格:¥2480.0
    规格:1mg产品价格:¥990.0
    基本信息
    产品类型多肽
    CASNo.141801-26-5
    单字母序列YPFF-NH2
    三字母序列Tyr-Pro-Phe-Phe-NH2
    别名内MOP肽 2;EndoMor-phin-2
    分子式C32H37N5O5
    分子量571.68
    纯度≥95%
    外观(性状)冻干粉;Lyophilized powder
    盐体系TFA盐;Trifluoroacetate salt
    来源合成;Synthetic
    储存条件Store at -20℃,2 years.(Avoid freeze/thaw cycles)
    类别/标签opium肽(opioid peptides)
    规格EndoMor-phin 2,一种高度选择性的高亲和力μ-opioid受体激动剂 , 对kappa3结合位点具有高亲和力 ,Ki为 20 到 30 nM 之间。EndoMor-phin 2, a high affinity, highly selective agonist of the μ-opioid receptor, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM.
    In VitroEndoMor-phin 2 is an endogenous opioid peptide and one of the two EndoMor-phins. It is a high affinity, highly selective agonist of the μ-opioid receptor, and along with EndoMor-phin 1 (EM-2). The two EndoMor-phins display reasonable affinities for kappa3 binding sites, with Ki values between 20 and 30 nM. EndoMor-phin 1 and EndoMor-phin 2 compete both μ1 and μ2 receptor sites quite potently. EndoMor-phins have little appreciable affinity for either delta or kappa1 binding sites, with Ki values greater than 500 nM.
    In VivoBoth EndoMor-phin 1 and EndoMor-phin 2 are potent analgesics with peak effects seen at 10 and 15 min, respectively. All subsequent studies are performed at peak effect. Both compounds are fully active supraspinally and spinally, with no indication of ceiling effects. EndoMor-phin 1 is significantly more potent spinally than supraspinally and, at the spinal level, it is significantly more potent than EndoMor-phin 2. The response of both agents are readily reversed by nalo-xone. β-FNA, a highly selective μ antagonist, effectively reverses the actions of both EndoMor-phins. Neither compound have analgesic activity in CXBK mice at a dose which produced over 70% analgesia in control CD-1 mice.
    单位

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