• 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
首页- Products - GPCR/G Protein - PAR - PAR-4 Agonist Peptide, amide

PAR-4 Agonist Peptide, amide

CAS No. 352017-71-1

PAR-4 Agonist Peptide, amide ( PAR-4-AP; AY-NH2 )

产品货号. M29763 CAS No. 352017-71-1

PAR-4 agonist peptide stimulates thromboxane production by human platelets with the maximal response to this agonist being approximately half of that observed after maximal thrombin stimulation.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1058 有现货
10MG ¥1778 有现货
25MG ¥3010 有现货
50MG ¥4291 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货

生物学信息

  • 产品名称
    PAR-4 Agonist Peptide, 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
    PAR-4 agonist peptide stimulates thromboxane production by human platelets with the maximal response to this agonist being approximately half of that observed after maximal thrombin stimulation.
  • 产品描述
    PAR-4 agonist peptide stimulates thromboxane production by human platelets with the maximal response to this agonist being approximately half of that observed after maximal thrombin stimulation.(In Vivo):Compared with their BALB/cBy controls, SCID mice have a significantly greater abdominal response to colorectal distension (CRD) at the distension levels of 0.04 to 0.1 mL increasing the intensity of EMG response by 384% to 132%, respectively (P<0.01; P<0.01; P<0.01; P<0.001). PAR-4 activation effectively reverses this hypersensitivity (P<0.01, P<0.05; P<0.05; P<0.05) .
  • 体外实验
    ——
  • 体内实验
    Compared with their BALB/cBy controls, SCID mice have a significantly greater abdominal response to colorectal distension (CRD) at the distension levels of 0.04 to 0.1 mL increasing the intensity of EMG response by 384% to 132%, respectively (P<0.01; P<0.01; P<0.01; P<0.001). PAR-4 activation effectively reverses this hypersensitivity (P<0.01, P<0.05; P<0.05; P<0.05) .
  • 同义词
    PAR-4-AP; AY-NH2
  • 通路
    GPCR/G Protein
  • 靶点
    PAR
  • 受体
    PAR-4
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    352017-71-1
  • 分子量
    680.79
  • 分子式
    C34H48N8O7
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (146.89 mM)
  • SMILES
    ——
  • 化学全称
    Sequence:Ala-Tyr-Pro-Gly-Lys-Phe-NH2

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

Annaházi A, et al. Proteinase-activated receptor-4 evoked colorectal analgesia in mice: an endogenously activatedfeed-back loop in visceral inflammatory pain. Neurogastroenterol Motil. 2012 Jan;24(1):76-85, e13.
产品手册
关联产品
  • Atopaxar hydrobromid...

    一种有效的、可逆的 PAR-1 拮抗剂,IC50 为 19 nM;对凝血酶和 TRAP 诱导的人血小板聚集具有有效的抑制作用,IC50 分别为 64 nM 和 31 nM。

  • Atopaxar

    一种有效的、可逆的 PAR-1 拮抗剂,IC50 为 19 nM;对凝血酶和 TRAP 诱导的人血小板聚集具有有效的抑制作用,IC50 分别为 64 nM 和 31 nM。

  • tcY-NH2

    Selective PAR4 antagonist peptide. Inhibits endostatin release and platelet aggregation induced by thrombin.