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PMX53

CAS No. 219639-75-5

PMX53 ( PMX 53 | Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg )

产品货号. M13502 CAS No. 219639-75-5

PMX53 (Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg)) 是一种有效的 C5a 受体 (CD88) 拮抗剂,IC50 为 20 nM。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
25MG ¥5581 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
1G 获取报价 有现货

生物学信息

  • 产品名称
    PMX53
  • 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
    PMX53 (Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg)) 是一种有效的 C5a 受体 (CD88) 拮抗剂,IC50 为 20 nM。
  • 产品描述
    PMX53 (Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg)) is a potent C5a receptor (CD88) antagonist with IC50 of 20 nM, also is an agonist for Mas-related gene 2 (MrgX2) in human mast cells; PMX-53 (10 nM) inhibited C5a-induced Ca(2+) mobilization in HMC-1 cells, but at higher concentrations (>30 nM) it caused degranulation in LAD2 mast cells, CD34(+) cell-derived mast cells, and RBL-2H3 cells stably expressing MrgX2; inhibits zymosan-, carrageenan-, LPS- and antigen-induced hypernociception in rats.
  • 体外实验
    ——
  • 体内实验
    Animal Model:Adult male Wistar rats (weighing 180-200?g) injected with zymosan Dosage:0.3 mg/kg, 1 mg/kg or 3?mg/kg Administration:Subcutaneous injection; once Result:Inhibited the hypernociception induced by zymosan-activated serum and C5a.
  • 同义词
    PMX 53 | Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg
  • 通路
    Immunology/Inflammation
  • 靶点
    Complement System
  • 受体
    Complement System
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    219639-75-5
  • 分子量
    896.1
  • 分子式
    C47H65N11O7
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 200 mg/mL (223.19 mM)
  • SMILES
    N=C(NCCC[C@H](NC([C@@H](NC([C@H](NC([C@H]1N(CCC1)C([C@@H](NC([C@@H](NC(C)=O)CC2=CC=CC=C2)=O)CCCN3)=O)=O)CC4CCCCC4)=O)CC5=CNC6=C5C=CC=C6)=O)C3=O)N
  • 化学全称
    Ac-Phe-cyclo(Orn-Pro-D-Cha-Trp-Arg)

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

1. Ting E, et al. Br J Pharmacol. 2008 Mar;153(5):1043-53. 2. Subramanian H, et al. Mol Pharmacol. 2011 Jun;79(6):1005-13. 3. Liu H, et al. Nat Struct Mol Biol. 2018 Jun;25(6):472-481. 4. Finch AM, et al. J Med Chem. 1999 Jun 3;42(11):1965-74.
产品手册
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