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Cat. No. | Product Name | Target | Signaling Pathways |
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T16481 |
PF-04995274
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
PF-04995274 是强效,高亲和力,口服活性血清素 4 受体的部分激动剂。它是可脑渗透的,可用于与阿尔茨海默症相关的认知障碍的研究。 | |||
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。 | |||
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. | |||
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]. | |||
T40778 |
Tyrosylleucine TFA
Tyr-Leu TFA |
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Tyrosylleucine (Tyr-Leu, YL) TFA is a dipeptide compound with potent antidepressant-like activity. This orally active compound demonstrates effective modulation of depressive symptoms. | |||
T40849 |
C20 Ceramide
N-Arachidoyl-D-sphingosine |
Endogenous Metabolite | Metabolism |
C20 Ceramide (N-Arachidoyl-D-sphingosine) 是一种存在于大脑中的 20:0 神经酰胺,可穿越血脑屏障激活小胶质细胞,诱导抑郁样行为。 | |||
T71537 | Tofenacin hydrochloride | ||
Tofenacin hydrochloride is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients. | |||
T79229 | ETAP | Monoamine Oxidase | Neuroscience |
ETAP为一种既抑制MAO-A也抑制MAO-B的化合物,展现出抗抑郁样活性,可应用于重度抑郁症的研究领域。 | |||
T70487 |
Tofenacin (free base)
|
||
Tofenacin (free base) is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients. | |||
T70174 |
Pirlindole-d4 HCl
|
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Pirlindole-d4 is intended for use as an internal standard for the quantification of pirlindole by GC- or LC-MS. Pirlindole is a selective and reversible monoamine oxidase A (MAO-A) inhibitor. It is selective for MAO-A over MAO-B. In rats, it reverses the depressive-like effects induced by chronic mild stress (CMS), increases proliferation of hippocampal neural progenitor cells, and reverses dendritic atrophy in granule neurons. Pirlindole is also an inhibitor of enterovirus-D68 and coxsackieviru... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T3933 |
Jatrorrhizine
Yatrorizine,neprotin,药根碱 |
MAO; 5-HT Receptor; Antibacterial; AChE | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Jatrorrhizine (neprotin) 是一种从黄连中分离得到的生物碱,具有抗菌、抗氧化、抗疟原虫和神经保护活性。它通过抑制 uptake-2 transporter 的活性减少血清素和去甲肾上腺素的摄取。它是一种有口服活性的乙酰胆碱酯酶制剂。 | |||
T4912 |
Jatrorrhizine chloride
盐酸药根碱,Yatrorhizine chloride,Neprotine chloride |
Others; 5-HT Receptor; OCT; Antibacterial; AChE | GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Others |
Jatrorrhizine chloride (Neprotine chloride) 是从黄连中分离得到的生物碱,具有神经保护、抗菌、抗氧化和抗疟原虫活性。它通过抑制摄取2转运蛋白的活性减少血清素和去甲肾上腺素的摄取。它是具有口服活性的乙酰胆碱酯酶抑制剂。 |