Cat. No. | Product Name | Target | Signaling Pathways |
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T10075 |
2-Methyl-5-HT
2-Methyl-5-hydroxytryptamine,2-甲基-5-羟基色氨酸盐酸 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
2-Methyl-5-HT (2-Methyl-5-hydroxytryptamine) 是5-HT3受体的选择性激动剂,显示出抗抑郁样作用。 | |||
T10075L |
2-Methyl-5-HT maleate
2-Methylserotonin maleate,2-Methyl-5-hydroxytryptamine maleate,2-Me-HT maleate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
2-Methyl-5-HT maleate (2-Methyl-5-hydroxytryptamine maleate) is a potent and selective 5-HT3 receptor agonist, which is shown to display anti-depressive-like effects[1]. | |||
T10075L2 |
2-Methyl-5-HT hydrochloride
2-Methyl-5-hydroxytryptamine hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
2-Methyl-5-HT hydrochloride (2-Methyl-5-hydroxytryptamine) is a potent and selective 5-HT3 receptor agonist with anti-depressive-like effects. | |||
T10170 |
5-HT7 agonist 1
4-[4-[(2-chlorophenyl)methyl]-1-piperazinyl]-1H-indole,4-[4-[(2-chlorophenyl)methyl]piperazin-1-yl]-1H-indole,4-[4-(2-chlorobenzyl)piperazino]-1H-indole |
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT7 agonist 1 (4-[4-[(2-chlorophenyl)methyl]piperazin-1-yl]-1H-indole)是一种5-HT7的选择性激动剂(IC50=222.93 nM)。5-HT7 agonist 1可用于有关中枢神经系统疾病的研究。 | |||
T9846 |
5-HT3 antagonist 5
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5-HT3 antagonist 5 是喹喔啉 -2- 甲酰胺化合物,是一种5-HT3受体拮抗剂。5-HT3 antagonist 5 对5-HT3激动剂和2-甲基-5-HT 也具有拮抗作用,并在小鼠中表现出抗抑郁作用。 | |||
T27607 |
Indisetron Dihydrochloride
N3389T,Sinseron,N-3389T,N 3389T |
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Indisetron Dihydrochloride is a 5-HT(3) and 5-HT(4) receptor antagonist. Indisetron reduces 2-methyl-5-serotonin (HT)-induced bradycardia. | |||
T70729 |
Indisetron
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Indisetron is a 5-HT(3) and 5-HT(4) receptor antagonist. Indisetron reduces 2-methyl-5-serotonin (HT)-induced bradycardia. | |||
T8437 | 3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox | Others | Others |
3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox 拮抗 2-methyl-5-HT 诱导的豚鼠回肠收缩。 | |||
T36521 |
Alaproclate (hydrochloride)
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Alaproclate is a selective serotonin reuptake inhibitor (SSRI).1,2 It inhibits depletion of serotonin (5-HT) induced by 4-methyl-α-ethyl-m-tyramine in rat cerebral cortex, hippocampus, hypothalamus, and striatum (EC50s = 18, 4, 8, and 12 mg/kg, respectively).1 Alaproclate inhibits NMDA-evoked currents and depolarization-induced voltage-dependent potassium currents in rat hippocampal neurons (IC50s = 1.1 and 6.9 μM, respectively) and does not inhibit GABA-evoked currents when used at concentratio... |