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78950-78-4

中文名稱(chēng) 8-OH-DPAT
英文名稱(chēng) S(-)-8-HYDROXY-DPAT HYDROBROMIDE PARTIAL 5-HT1A SECROT
CAS 78950-78-4
分子式 C16H26BrNO
分子量 328.288
MOL 文件 78950-78-4.mol
更新日期 2025/01/14 09:39:19
78950-78-4 結(jié)構(gòu)式 78950-78-4 結(jié)構(gòu)式

基本信息

中文別名
化合物8-OH-DPAT
英文別名
3-(dipropylamino)tetralin-5-ol
7-(dipropylamino)tetralin-1-ol
2-(Dipropylamino)tetralin-8-ol
8-Hydroxy-2-(di-n-propylamino)tetralin
S(-)-8-Hydroxy-DPAT hydrobromide solid
7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-ol
5,6,7,8-Tetrahydro-7-(dipropylamino)naphthalen-1-ol
(+/-)-8-Hydroxy-2-dipropylaminotetralinehydrobromide
1-Naphthalenol,7-(dipropylamino)-5,6,7,8-tetrahydro-
S(-)-8-HYDROXY-DPAT HYDROBROMIDE PARTIAL 5-HT1A SECROT

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度150mg/ml in DMSO
形態(tài)固體
顏色白色
旋光性 (optical activity)[α]25/D 67.8° in methanol(lit.)

安全數(shù)據(jù)

安全說(shuō)明22-24/25
WGK Germany3

常見(jiàn)問(wèn)題列表

生物活性
8-OH-DPAT 是一種有效的,選擇性的 5-HT 激動(dòng)劑,對(duì) 5-HT1A 的 pIC50 值為 8.19,對(duì) 5-HT7 的 Ki 值為 466 nM,對(duì) 5-HT1B (pIC50, 5.42) 和 5-HT (pIC50 <5) 的作用很弱。
靶點(diǎn)

5-HT 1A Receptor

8.19 (pIC 50 )

5-HT 7 Receptor

466 nM (Ki)

體外研究

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.

體內(nèi)研究

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.

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