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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14767 |
BP 897 hydrochloride
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
BP 897 hydrochloride 是有效的部分多巴胺 D3受体激动剂和弱 D2受体拮抗剂,在多巴胺 D3 受体 (Ki=0.92 nM) 上显示出高亲和力,而在 D2 受体上显示出 70 倍的低亲和力 (Ki=61 nM)。它表现出对可卡因寻求行为的选择性抑制。 | |||
T9100 |
BP 897
2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]- |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
BP 897 (2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]-) 是一种有效的部分多巴胺D3受体激动剂和弱D2受体拮抗剂,在多巴胺 D3 受体(Ki=0.92 nM) 上显示出高亲和力,而在 D2 受体上显示出 70 倍的低亲和力 (Ki=61 nM)。它表现出对可卡因寻求行为的选择性抑制。 | |||
T4385 |
PF-4840154
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
PF4840154 是有效的大鼠和人TrpA1通道选择性激动剂,EC50分别为 97 和 23 nM。PF-4840154 可以诱导 TrpA1 介导的小鼠伤害行为。 | |||
T38001 |
LEI-401
LEI 401 |
Phospholipase | Metabolism |
LEI-401 是一种可穿过血脑屏障且具有选择性和有效性的 NAPE-PLD 抑制剂(IC50:27 nM)。LEI-401 降低自由活动小鼠脑内n -酰基乙醇胺(NAEs)含量,可调节小鼠情绪行为。 | |||
T28282 |
Oxypertine
Win-18501,Forit,Win18501,Win 18501 |
Others | Others |
Oxypertine is an indole-derivative antipsychotic with general properties similar to those of the chlorpromazine and phenothiazine. Oxypertine is used as a treatment for various psychoses including mania, schizophrenia, disturbed behaviour, and severe anx | |||
T26807 |
Bifeprunox Mesylate
Bifeprunox,DU 127090,DU-127090,DU127090 |
Others | Others |
Bifeprunox is a partial dopamine and serotonin agonist potentially for the treatment of schizophrenia. Bifeprunox suppresses in vivo VTA dopaminergic neuronal activity via D2 and not D3 dopamine autoreceptor activation. Bifeprunox influences nicotine-seek | |||
T27752 |
KT109
KT-109,KT 109 |
Others | Others |
KT109 is a selective inhibitor of DAGLβ (IC50 = 42 nM). KT109-treated wild-type mice displayed reductions in LPS-induced allodyni as well as in DAGL-β (-/-) micea. Repeated KT109 administration prevented the expression of LPS-induced allodynia, without ev | |||
T62132 |
S-777469
|
Others | Others |
S-777469 是一种选择性的、口服具有活力的大麻素 2 型受体(CB2)激动剂 (Ki: 36 nM)。S-777469 能够剂量依赖性地明显抑制化合物 48/80 诱导的小鼠抓挠行为。S-777469 兴奋 CB2,抑制瘙痒信号的传递,显示出止痒效果。 | |||
T38145 |
Eltoprazine
|
Others | Others |
Eltoprazine(DU28853) is a serenic or antiaggressive agent which as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor.IC50 value:Target: 5-HT1A/1B agonist; 5-HT2C antagonistin vitro: The binding of [3H]eltoprazine to whole tissue sections was saturable and revealed an apparent dissociation constant (Kd) of 11 nM. Specific [3H]eltoprazine binding was completely displaced by 5-HT; conversely, unlabelled eltoprazine reduced [3H]5-HT binding to the levels of no... |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02393 |
Thimet Oligopeptidase/THOP1 Protein, Mouse, Recombinant (His)
thimet oligopeptidase 1,EP24.15,AI131655,AI327041 |
Mouse | Baculovirus Insect Cells |
THOP1, also known as Thimet oligopeptidase 1, Thimet oligopeptidase, EC 3.4.24.15, or EP24.15, is a zinc(II) endopeptidase implicated in the processing of numerous physiological peptides. As an intracellular enzyme, highly expressed in the brain, kidneys and neuroendocrine tissue, THOP1 has been proposed to metabolize peptides within cells, thereby affecting antigen presentation and G protein-coupled receptor signal transduction. Its substrates is gonadotrophin-releasing hormone (GnRH), an impor... |