质量水平
检测方案
≥98%
SMILES字符串
Br[H].CCCN(CCC)C1CCc2cccc(O)c2C1
InChI
1S/C16H25NO.BrH/c1-3-10-17(11-4-2)14-9-8-13-6-5-7-16(18)15(13)12-14;/h5-7,14,18H,3-4,8-12H2,1-2H3;1H
InChI key
BATPBOZTBNNDLN-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
(±)-8-羟基-2-(二丙基氨基)四氢溴酸盐是一种强效的选择性 5-羟色胺 (5HT 1A )-受体激动剂 ,通常作为药理学研究的标准。
生化/生理作用
选择性 5-HT1 激动剂,对亚型 5-HT1A 受体具有高亲和性。
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
8-Hydroxy-2-(dipropylamino) tetralin, a new centrally acting 5-hydroxytryptamine receptor agonist.
Journal of Medicinal Chemistry, 24(8), 921-923 (1981)
Improved preparation, chromatographic separation and X-ray crystallographic determination of the absolute configuration of the enantiomers of 8-hydroxy-2-(dipropylamino) tetralin (8-OH DPAT).
Acta Chemica Scandinavica, 42, 231-236 (1988)
Arylpiperazine agonists of the serotonin 5-HT 1A receptor preferentially activate cAMP signaling versus recruitment of β-arrestin-2.
Bioorganic & Medicinal Chemistry, 23(15), 4824-4830 (2015)
eLife, 10 (2021-06-04)
Consolation is a common response to the distress of others in humans and some social animals, but the neural mechanisms underlying this behavior are not well characterized. By using socially monogamous mandarin voles, we found that optogenetic or chemogenetic inhibition
Journal of neurochemistry, 47(2), 529-540 (1986-08-01)
Drug interactions with 5-HT1 (5-hydroxytryptamine type 1) binding site subtypes were analyzed in rat frontal cortex. 8-Hydroxy-N,N-dipropyl-2-aminotetralin (8-OH-DPAT) displays high affinity (Ki 3.3 +/- 1 nM) for 29 +/- 3% of total [3H]5-HT binding in rat frontal cortex and low
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门