货号 | 5645/10 |
别名 | 2-(1H-Indol-3-ylmethyl)-9-(4-methox |
供应商 | Tocris |
生物活性 | OX2 receptor antagonist. Exhibits approximately six-fold selectivity for OX2 versus OX1 receptors. Decreases activity and increases sleep time in mice during the active phase, without affecting REM/NREM balance. Orally bioavailable. Brain penetrant. |
运输条件 | Blue Ice |
存放说明 | 4℃ |
纯度 | >98 % |
计算分子量 | 405.49 |
分子式 | C23H27N5O2 |
可溶性/溶解性 | Soluble to 100 mM in DMSO and to 100 mM in 1eq. HCl |
参考文献 | Betschartet al (2013) Identification of a novel series of orexin receptor antagonists with a distinct effect on sleep architecture for the treatment of insomnia. J.Med.Chem. 56 7590. PMID: 23964859. Hoyeret al (2013) Distinct effects of IPSU and suvorexant on mouse sleep architecture. Front.Neurosci. 7 230. PMID: 24376396. |