常用名 | 2-(2-(1-萘甲酰基)-8-氟-1.2.3.4-四氢吡啶并[4,3-B]吲哚-5基)乙酸 | CAS号 | 866460-33-5 |
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价格 | ¥需询单/1kg ¥需询单/1g | 纯度 | 99.0% |
备货期 | 需询单 | 库存 | 询单 |
产品详情(用途,包装等)
用途: Setipiprant is an orally available, selective CRTH2 antagonist. CRTH2 is a G protein-coupled receptor for PGD2.IC50 value: 6.0 nMTarget: PGD2in vitro: Setipiprant is an orally available, selective CRTH2 (chemoattractant receptor-homologous molecule expressed on T helper [Th]-2 cells) antagonist. 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. Thus, antagonism of CRTH2 receptors is considered to be a promising therapeutic target for various allergic diseases and asthma. 物理化学性质: CAS号:866460-33-5 常用中文名:2-(2-(1-萘甲酰基)-8-氟-1.2.3.4-四氢吡啶并[4,3-B]吲哚-5基)乙酸 常用英文名:Setipiprant 分子式:C24H19FN2O3 分子量:402.418 密度:1.4±0.1 g/cm3 沸点:690.4±55.0 °C at 760 mmHg 熔点:N/A 闪点:371.4±31.5 °C 储存条件:-20℃ |