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Setipiprant

CAS No. 866460-33-5

Setipiprant ( ACT-129968 | ACT 129968 | KYTH 105 | Setipiprant )

产品货号. M19195 CAS No. 866460-33-5

Setipiprant 是一种口服的选择性 CRTH2 拮抗剂 (IC50: 6.0 nM)。 CRTH2 是前列腺素 (PGD2) 的 G 蛋白偶联受体。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥125 有现货
5MG ¥188 有现货
10MG ¥264 有现货
25MG ¥415 有现货
50MG ¥644 有现货
100MG ¥981 有现货
200MG ¥1404 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥240 有现货

生物学信息

  • 产品名称
    Setipiprant
  • 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
    Setipiprant 是一种口服的选择性 CRTH2 拮抗剂 (IC50: 6.0 nM)。 CRTH2 是前列腺素 (PGD2) 的 G 蛋白偶联受体。
  • 产品描述
    Setipiprant is an orally available, selective CRTH2 antagonist (IC50: 6.0 nM). CRTH2 is a G protein-coupled receptor for prostaglandin (PGD2). PGD2 is produced by the mast cells and is a key mediator in various inflammatory diseases, including allergy and asthma. Binding of PGD2 to CRTH2, which are expressed on the surface of blood-borne cells, induces chemotaxis of Th2 cells, basophils, and eosinophils, and stimulates cytokine release from these cells.(In Vitro):Setipiprant (0-10 μM; 90 min) interacts with hCRTH2 receptor in the absence and presence of Human Serum Albumin (HSA) in the assay buffer with IC50 values of 6 and 340 nM, respectively.Setipiprant (0-10 μM; 5-20 min) inhibits hCRTH2 receptor based intracellular calcium liberation, intracellular cAMP and shape change of human eosinophils with IC50 values of 30, 80 and 235 nM, respectively.Setipiprant (0-10 μM) inhibits prostanoid receptors hDP1, hEP2 and hEP4 with IC50 values of 1290, 2600 and >10000 nM, respectively.(In Vivo):Pharmacokinetic Properties of Setipiprant in Rats and Dogs.
  • 体外实验
    Setipiprant (0-10 μM; 90 min) interacts with hCRTH2 receptor in the absence and presence ofHuman Serum Albumin (HSA) in the assay buffer with IC50 values of 6 and 340 nM, respectively.Setipiprant (0-10 μM; 5-20 min) inhibits hCRTH2 receptor based intracellular calcium liberation, intracellular cAMP and shape change of human eosinophils with IC50 values of 30, 80 and 235 nM, respectively.Setipiprant (0-10 μM) inhibits prostanoid receptors hDP1, hEP2 and hEP4 with IC50 values of 1290, 2600 and >10000 nM, respectively.
  • 体内实验
    ——
  • 同义词
    ACT-129968 | ACT 129968 | KYTH 105 | Setipiprant
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    CRTh2
  • 研究领域
    Inflammation/Immunology
  • 适应症
    ——

化学信息

  • CAS Number
    866460-33-5
  • 分子量
    402.42
  • 分子式
    C24H19FN2O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 36 mg/mL; 89.46 mM
  • SMILES
    C1CN(CC2=C1N(C3=C2C=C(C=C3)F)CC(=O)O)C(=O)C4=CC=CC5=CC=CC=C54
  • 化学全称
    2-(2-(1-naphthoyl)-8-fluoro-1,2,3,4-tetrahydro-5H-pyrido[4,3-b]indol-5-yl)acetic acid

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. Diamant Z., et al. Setipiprant, a selective CRTH2 antagonist, reduces allergen-induced airway responses in allergic asthmatics. Clin Exp Allergy. 2014 Aug;44(8):1044-52.
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