2-(3,5-Bis(Trifluoromethyl)Phenyl)-N,2-Dimethyl-N-(6-(4-Methylpiperazin-1-Yl)-4-(O-Tolyl)Pyridin-3-Yl)Propanamide 2-(3,5-双(三氟甲基)苯基)-N,2-二甲基-N-(6-(4-甲基哌嗪-1-基)-4-(邻甲苯基)吡啶-3-基)丙酰胺
CAS 290297-26-6 MFCD90297266
化学结构图
SMILES:
化学属性
| Mol. Formula | C30H32F6N4O |
|---|
别名和识别编码
| Chemical Name | 2-(3,5-Bis(Trifluoromethyl)Phenyl)-N,2-Dimethyl-N-(6-(4-Methylpiperazin-1-Yl)-4-(O-Tolyl)Pyridin-3-Yl)Propanamide |
|---|---|
| Chemical Name Translation | 2-(3,5-双(三氟甲基)苯基)-N,2-二甲基-N-(6-(4-甲基哌嗪-1-基)-4-(邻甲苯基)吡啶-3-基)丙酰胺 |
| Chemicalbook ID | CB71483126 |
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相关文献及参考
- [2]. Rizzi A, et al. In vitro and in vivo pharmacological characterization of the novel NK1 receptor selective antagonist Netupitant. Peptides. 2012 Sep;37(1):86-97.
- [3]. Stefano Palea, et al. Netupitant, a Potent and Highly Selective NK1 Receptor Antagonist, Alleviates Acetic Acid-Induced Bladder Overactivity in Anesthetized Guinea-Pigs. Front Pharmacol. 2016 Aug 4;7:234.
- [1]. Hoffmann T, et al. Design and synthesis of a novel, achiral class of highly potent and selective, orally active neurokinin-1 receptor antagonists. Bioorg Med Chem Lett. 2006 Mar 1;16(5):1362-5.
- [1]. Hoffmann T, et al. Design and synthesis of a novel, achiral class of highly potent and selective, orally active neurokinin-1 receptor antagonists. Bioorg Med Chem Lett. 2006 Mar 1;16(5):1362-5.
- [2]. Rizzi A, et al. In vitro and in vivo pharmacological characterization of the novel NK1 receptor selective antagonist Netupitant. Peptides. 2012 Sep;37(1):86-97.
- [3]. Stef
