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形狀
solid
光學活性
[α]25/D +81.4°, c = 0.30 in methanol(lit.)
顏色
white
溶解度
H2O: slightly soluble
ethanol: soluble
SMILES 字串
Cl[H].CCCN(CCC)[C@@H]1CCc2c(F)ccc(O)c2C1
InChI
1S/C16H24FNO.ClH/c1-3-9-18(10-4-2)12-5-6-13-14(11-12)16(19)8-7-15(13)17;/h7-8,12,19H,3-6,9-11H2,1-2H3;1H/t12-;/m1./s1
InChI 密鑰
FKUVCCNCUAFKAH-UTONKHPSSA-N
基因資訊
human ... HTR1A(3350)
生化/生理作用
R(+)-UH-301 hydrochloride is a potent and selective 5-HT1A serotonin receptor agonist. R(+)-UH-301 is also known to function as an antinociceptive agent, as it has been shown to significantly decrease formalin-induced flinching in rats.
注意
Hygroscopic, photosensitive
準備報告
R(+)-UH-301 hydrochloride is soluble in ethanol and is slightly soluble in water.
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2(2), 141-147 (1992-06-01)
The effects of the enantiomers of 5-fluoro-8-hydroxy-2-(dipropylamino)tetralin, UH-301 and the potent 5-HT1A-receptor agonist (R)-8-hydroxy-2-(dipropylamino)tetralin, (R)-8-OH-DPAT, on locomotion, rearing and total activity were studied in rats. The experiments were performed as tests either of exploratory activity in non-habituated rats or of
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2(2), 127-133 (1992-06-11)
In this study, we examined the effects of acute and chronic administration of the 5-HT3 receptor antagonist granisetron (0.1, 1.0 or 10 mg/kg i.p.) alone or in combination with haloperidol (0.5 mg/kg i.p.) on the number of spontaneously active dopamine
Neuroscience, 165(2), 561-568 (2009-10-20)
This study assessed the possible antinociceptive role of peripheral 5-HT(1) receptor subtypes in the rat formalin test. Rats were injected into the dorsum of the hind paw with 50 microl of diluted formalin (1%). Nociceptive behavior was quantified as the
Nature chemical biology, 3(5), 268-273 (2007-04-10)
The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain cancer. However, the complete repertoire of signaling pathways that governs the
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