8-OH-DPAT
中文名称 | 8-OH-DPAT |
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中文同义词 | 化合物8-OH-DPAT;8-羟基-DPAT |
英文名称 | S(-)-8-HYDROXY-DPAT HYDROBROMIDE PARTIAL 5-HT1A SECROT |
英文同义词 | S(-)-8-HYDROXY-DPAT HYDROBROMIDE PARTIAL 5-HT1A SECROT;(+/-)-8-Hydroxy-2-dipropylaminotetralinehydrobromide;7-(dipropylamino)tetralin-1-ol;8-Hydroxy-2-(di-n-propylamino)tetralin;2-(Dipropylamino)tetralin-8-ol;2-(N,N-Dipropylamino)-1,2,3,4-tetrahydronaphthalen-8-ol;5,6,7,8-Tetrahydro-7-(dipropylamino)naphthalen-1-ol;8-Hydroxy-2-(dipropylamino)-1,2,3,4-tetrahydronaphthalene |
CAS号 | 78950-78-4 |
分子式 | C16H25NO |
分子量 | 247.38 |
EINECS号 | |
相关类别 | Serotonin receptor |
Mol文件 | 78950-78-4.mol |
结构式 |
8-OH-DPAT 性质
沸点 | 372.5±42.0 °C(Predicted) |
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密度 | 1.03±0.1 g/cm3(Predicted) |
储存条件 | Store at -20°C |
溶解度 | 150mg/ml DMSO 溶液 |
形态 | 固体 |
酸度系数(pKa) | 10.54±0.40(Predicted) |
颜色 | 白色 |
旋光性 (optical activity) | [α]25/D 67.8° in methanol(lit.) |
5-HT 1A Receptor 8.19 (pIC 50 ) |
5-HT 7 Receptor 466 nM (Ki) |
8-OH-DPAT is a potent and selective 5-HT agonist, with a pIC 50 of 8.19 for 5-HT1A; weakly binds to 5-HT1B (pIC 50 , 5.42), 5-HT (pIC 50 <5). 8-OH-DPAT has high affinity at 5-HT7 with a K i of 466 nM, and does not bind to 5-HT6 or 5-HT4.
8-OH-DPAT (1 mg/kg) normalizes hypolocomotion, significantly increases wakefulness and reduces the duration of REM sleep without effect on the duration of non-REM sleep in the dark period in orexin knockout (KO) mice. 8-OH-DPAT shows no obvious effect on wakefulness or the duration of either REM sleep or non-REM sleep in WT mice. 8-OH-DPAT (1 mg/kg, s.c.) activates 5-HT1A receptor in orexin knockout mice.
安全信息
安全说明 | 22-24/25 |
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WGK Germany | 3 |