简介:SAR191801 抑制剂是一种hPGDS抑制剂, 荧光偏振检测或EIA法测得IC50值为12 nM。
SAR191801 抑制剂物理化学性质:
分子式 |
C22H20N6O3 |
分子量 |
416.433 |
精确质量 |
416.16 |
PSA |
126.92 |
LogP |
3.1369 |
SAR191801 抑制剂详细介绍:
中文名称: |
SAR191801 抑制剂 |
中文别名: |
N-[[3-[5-(1-羟基-1-甲基乙基)-1,2,4-恶二唑-3-基]苯基]甲基]-2-(2-吡啶基)-5-嘧啶甲酰胺 |
英文名称: |
SAR191801 |
英文别名: |
SAR191801;hPGDS-IN-1 |
CAS号: |
1234708-04-3 |
分子式: |
C22H20N6O3 |
分子量: |
416.43 |
详细描述: |
博飞美科提供1234708-04-3,SAR191801 抑制剂,SAR191801,Perfemiker,上海现货。 Medlife,致力于提供高品质、高性价比小分子化合物的产品。 Medlife小分子化合物大量库存,提供超过2万种的抑制剂、激动剂、拮抗剂等产品,是药物及疾病研究的重要原料供应商。 hPGDS抑制剂。hPGDS-IN-1是一种hPGDS抑制剂, 荧光偏振检测或EIA法测得IC50值为12 nM。 查询关键词:“1234708-04-3,SAR191801 抑制剂,SAR191801,PC16813,Perfemiker,上海现货”。 |
SAR191801 抑制剂参考文献:
[1]. Vandeusen, Christopher L, et al. Phenyloxadiazole derivatives as PGD inhibitors and their preparation, pharmaceutical compositions and use in the treatment of allergic and inflammatory disorders. From PCT Int. Appl. (2011), WO 2011044307 A1 20110414.
[2]. Hahn Chang S. Method for treating macular degeneration using syk multikinase inhibitor, an hPGDS inhibitor and a DP antagonist. From PCT Int. Appl. (2010), WO 2010080563 A2 20100715.
[3]. Weiberth Franz J, et al. Demonstration on Pilot-Plant Scale of the Utility of 1,5,7-Triazabicyclo[4.4.0]dec-5-ene (TBD) as a Catalyst in the Efficient Amidation of an Unactivated Methyl Ester. From Organic Process Research & Development (2012), 16(12), 19