所有图片(1)
别名:
4-[2-[4-[3-(Trifluoromethyl)phenyl]-1-piperazinyl]ethyl]benzeneamine, p-Aminophenethyl-m-trifluoromethylphenyl piperazine, PAPP
经验公式（希尔记法）:
C19H22F3N3
推荐产品
形式
solid
质量水平
颜色
off-white
溶解性
0.1 M HCl: slightly soluble
H2O: insoluble
ethanol: freely soluble
SMILES字符串
Nc1ccc(CCN2CCN(CC2)c3cccc(c3)C(F)(F)F)cc1
InChI
1S/C19H22F3N3/c20-19(21,22)16-2-1-3-18(14-16)25-12-10-24(11-13-25)9-8-15-4-6-17(23)7-5-15/h1-7,14H,8-13,23H2
InChI key
GAAKALASJNGQKD-UHFFFAOYSA-N
基因信息
human ... HTR1A(3350) , HTR1D(3352)
生化/生理作用
Selective 5-HT1A serotonin receptor agonist and 5-HT1D serotonin receptor antagonist.
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Kosuke Ino et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 35(1), 39-43 (2018-10-03)
Tissue engineering requires analytical methods to monitor cell activity in hydrogels. Here, we present a method for the electrochemical imaging of cell activity in hydrogels embedded in printed polycaprolactone (PCL) scaffolds. Because a structure made of only hydrogel is fragile
M L Cohen et al.
Life sciences, 39(25), 2441-2446 (1986-12-22)
LY165163, a ligand reported to be selective for the 5HT1A subtype of serotonin receptor, was examined for its ability to interact with 5HT2 receptors in the rat jugular vein and alpha-receptors in the rat aorta. In these smooth muscle preparations
R W Ransom et al.
Journal of neurochemistry, 46(1), 68-75 (1986-01-01)
1-[2-(4-Aminophenyl)ethyl]-4-(3-trifluoromethylphenyl)piperazine (PAPP) inhibits [3H]5-hydroxytryptamine (5-HT, serotonin) binding to 5-HT1A and 5-HT1B sites in rat brain with apparent equilibrium dissociation constants (KD) of 2.9 and 328 nM, respectively. [3H]PAPP was synthesized, its binding to central serotonin receptors was examined, and its
Mingyi Cai et al.
Journal of agricultural and food chemistry, 58(5), 2624-2629 (2009-12-17)
1-[(4-Aminophenyl)ethyl]-4-[3-(trifluoromethyl)phenyl]piperazine (PAPP) is a 5-HT(1A) agonist and was reported to display high affinity for serotonin (5-HT) receptor from the parasitic nematode Haemonchus contortus . The present investigation explored the possibility of using PAPP as a lead compound of new insecticides
Electrophysiological responses of serotoninergic dorsal raphe neurons to 5-HT1A and 5-HT1B agonists.
J S Sprouse et al.
Synapse (New York, N.Y.), 1(1), 3-9 (1987-01-01)
A direct comparison was made of the effects of serotonin 5-HT1A and 5-HT1B selective compounds on the spontaneous firing rate of dorsal raphe serotoninergic neurons in chloral-hydrate-anesthetized rats. Following intravenous administration, the 5-HT1A selective compounds ipsapirone (TVX Q 7821) and
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