• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

γ-2-MSH (41-58), amide

CAS No. 799841-81-9

γ-2-MSH (41-58), amide ( —— )

产品货号. M30231 CAS No. 799841-81-9

Melanocortin (MC) 3-MSH (Melanocyte-Stimulating Hormone) is believed to signal through the MC 3 receptor. It induces a sustained increase in intracellular free calcium levels ([Ca2+]i) in a subpopulation of pituitary cells. Most of the cells responding to 3-MSH express more than one pituitary hormone mRNA. The effect of 3-MSH is blocked by SHU9119, a MC3R and MC4R antagonist, in only 50% of the responsive cells, suggesting that in half of these cells the mediating receptor is not the MC3R. Low picomolar doses of 3-MSH increase [Ca2+]i in the growth hormone (GH)- and prolactin (PRL)-secreting GH3 cell line.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    γ-2-MSH (41-58), amide
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Melanocortin (MC) 3-MSH (Melanocyte-Stimulating Hormone) is believed to signal through the MC 3 receptor. It induces a sustained increase in intracellular free calcium levels ([Ca2+]i) in a subpopulation of pituitary cells. Most of the cells responding to 3-MSH express more than one pituitary hormone mRNA. The effect of 3-MSH is blocked by SHU9119, a MC3R and MC4R antagonist, in only 50% of the responsive cells, suggesting that in half of these cells the mediating receptor is not the MC3R. Low picomolar doses of 3-MSH increase [Ca2+]i in the growth hormone (GH)- and prolactin (PRL)-secreting GH3 cell line.
  • 产品描述
    Melanocortin (MC) 3-MSH (Melanocyte-Stimulating Hormone) is believed to signal through the MC 3 receptor. It induces a sustained increase in intracellular free calcium levels ([Ca2+]i) in a subpopulation of pituitary cells. Most of the cells responding to 3-MSH express more than one pituitary hormone mRNA. The effect of 3-MSH is blocked by SHU9119, a MC3R and MC4R antagonist, in only 50% of the responsive cells, suggesting that in half of these cells the mediating receptor is not the MC3R. Low picomolar doses of 3-MSH increase [Ca2+]i in the growth hormone (GH)- and prolactin (PRL)-secreting GH3 cell line.
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    ——
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    799841-81-9
  • 分子量
    1569.79
  • 分子式
    C74H100N22O15S
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    ——
  • 化学全称
    Sequence:{Tyr}{Val}{Met}{Gly}{His}{Phe}{Arg}{Trp}{Asp}{Arg}{Phe}{Gly}

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

Joseph CG, et al. γ?-Melanocyte stimulation hormone (γ?-MSH) truncation studies results in the cautionary note that γ?-MSH is not selective for the mouse MC3R over the mouse MC5R. Peptides. 2010 Dec;31(12):2304-13.
产品手册
关联产品
  • m-PEG12-OH

    m-PEG12-OH 是一种基于 PEG 的 PROTAC 连接体,可用于 PROTAC 的合成。

  • Coumarin-3-carboxyli...

    丙戊酸与香豆素-3-羧酸的组合通过 EGFR/VEGFR2/c-Met-Akt-NF-κB 信号通路抑制肺癌细胞的增殖和迁移。

  • PROTAC PD-1/PD-L1 de...

    PROTAC PD-1/PD-L1 degrader-1,基于 Cereblon E3配体的 PD-1/PD-L1 PROTAC,抑制 PD-1/PD-L1 相互作用,IC50 为 39.2 nM。PROTAC PD-1/PD-L1 degrader-1 可显着恢复在 Hep3B/OS-8/hPD-L1 和 CD3 T 细胞共培养模型中抑制的免疫力。PROTAC PD-1/PD-L1 degrader-1 以溶酶体依赖性方式适度降低 PD-L1 的蛋白质水平。