购物车
- 全部删除
- 您的购物车当前为空
AZD1981 是一种有效且特异性的 CRTh2 (DP2) 受体拮抗剂,IC50为 4 nM,用于研究哮喘、绝经后、药代动力学、哮喘患者和药物相互作用等治疗和基础科学的试验。
为众多的药物研发团队赋能,
让新药发现更简单!
AZD1981 是一种有效且特异性的 CRTh2 (DP2) 受体拮抗剂,IC50为 4 nM,用于研究哮喘、绝经后、药代动力学、哮喘患者和药物相互作用等治疗和基础科学的试验。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 111 | 现货 | |
5 mg | ¥ 248 | 现货 | |
10 mg | ¥ 493 | 现货 | |
25 mg | ¥ 990 | 现货 | |
50 mg | ¥ 1,930 | 现货 | |
100 mg | ¥ 2,830 | 现货 | |
200 mg | ¥ 3,960 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 273 | 现货 |
产品描述 | AZD1981 is an effective and specific CRTh2 (DP2) receptor antagonist (IC50: 4 nM), showing >1000-fold selectivity over more than 340 other enzymes and receptors, including DP1. AZD1981 has been used in trials studying the treatment and basic science of Asthma, Postmenopausal, Pharmakokinetic, Asthma Patients, and Drug Interaction, among others. |
靶点活性 | CRTh2 (DP2) receptor:4 nM |
体外活性 | AZD1981, as a potent antagonist in a disease relevant cell system, inhibits DK-PGD2-induced CD11b expression in human eosinophils with IC50 of 10 nM. [1] AZD1981 blocks DP2-mediated shape change in human eosinophils and basophils in blood, as well as DP2-mediated chemotaxis of human Th2 cells and eosinophils. Moreover, AZD1981 also blocks the binding of [3H]PGD2 to mouse, rat, guinea pig, rabbit and dog recombinant DP2. [2] |
体内活性 | AZD1981 has high oral bioavailability in male sprague dawley rats. [1] In guinea pig hind limb model, AZD1981 (100 nM) completely inhibits DK-PGD2-induced eosinophil mobilization. [2] |
分子量 | 388.87 |
分子式 | C19H17ClN2O3S |
CAS No. | 802904-66-1 |
Smiles | CC(=O)Nc1cccc2n(CC(O)=O)c(C)c(Sc3ccc(Cl)cc3)c12 |
密度 | 1.37 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
溶解度信息 | Ethanol: < 1 mg/mL (insoluble or slightly soluble) H2O: < 1 mg/mL (insoluble or slightly soluble) DMSO: 9 mg/mL (23.1 mM) | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
|
版权所有©2015-2024 TargetMol Chemicals Inc.保留所有权利.
评论内容