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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T23513	VU10010 VU 10010	AChR	Neuroscience
	VU10010 (VU 10010) 是一种高度选择性的M4mAChR 变构增强剂，EC50为 400 nM。它与 M4mAChR 的变构位点结合，增强与 G 蛋白偶联，增加对乙酰胆碱的亲和力，还会增加卡巴胆碱引起的兴奋性传导抑制。
T0333	Aniracetam Ro 13-5057,阿尼西坦,茴拉西坦	Dopamine Receptor; 5-HT Receptor; GluR; AChR; iGluR	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Aniracetam (Ro 13-5057) 是一种促智和神经保护药物，可选择性地调节 AMPA 受体和 nAChR。
T0939	Phenytoin 苯妥英,Diphenylhydantoin,5,5-Diphenylhydantoin	Virus Protease; Sodium Channel	Membrane transporter/Ion channel; Microbiology/Virology
	Phenytoin (5,5-Diphenylhydantoin) 是一种有效的电压门控钠离子通道阻滞剂，可减少小鼠乳腺肿瘤的生长和转移，具有抗癫痫活性。
T20522	Acetylcholine perchlorate AI351678,AI3-51678,AI3 51678
	Acetylcholine perchlorate is the perchlorate salt of acetylcholine. Acetylcholine, an endogenous neurotransmitter at cholinergic synapses, could amplify the action potential of the sarcolemma following by inducing muscle contractions.
T76130	Acetylcholinesterase
	Acetylcholinesterase(ACHE; EC 3.1.1.7), 即乙酰胆碱酯酶，是一种胆碱能酶，主要存在于神经肌肉接头和胆碱能类型的化学突触中，常用于生化研究。Acetylcholinesterase 可以催化乙酰胆碱和其他一些充当神经递质的胆碱酯分解或水解为乙酸和胆碱。Acetylcholinesterase 主要作用是终止突触之间的神经元传递和信号传导，以防止 ACh 扩散和附近受体的激活。
T28653	S-8510 free base SB 737552,SB-737552,S8510,SB737552,S-8510,S 8510
	S-8510 is a GABA-A receptor inverse agonist. S-8510 selectively potentiated pentylenetetrazol-induced convulsion without affecting minimal electroconvulsive shock- or strychnine-induced convulsion in ddY mice. S-8510 ameliorated memory impairment induced
T76221	Leptin (116-130)
	Leptin(116-130)是一种生物活性的瘦素片段，能促进AMPA受体运输至突触并加强活动依赖性的海马突触可塑性。此外，Leptin(116-130)在抗淀粉样蛋白毒性模型中有效阻止海马突触损伤和神经元细胞死亡，显示出对研究阿尔茨海默病(AD)具有重要潜力。
T36679	Rp-cAMPS sodium salt
	Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis by phosphodiesterases[1][2][3][4][5][6]. A membrane-permeable competitive cAMP antagonist (Rp-cAMPS) that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme also inhibits synaptic plasticity but has no effect on normal synaptic t...

化合物

VU10010

Cat.No: T23513

Synonym: VU 10010

Target: AChR

Aniracetam

Cat.No: T0333

Synonym: Ro 13-5057,阿尼西坦,茴拉西坦

Target: Dopamine Receptor, 5-HT Receptor, GluR, AChR, iGluR

Phenytoin

Cat.No: T0939

Synonym: 苯妥英,Diphenylhydantoin,5,5-Diphenylhydantoin

Target: Virus Protease, Sodium Channel

Acetylcholine perchlorate

Cat.No: T20522

Synonym: AI351678,AI3-51678,AI3 51678

Synonym: SB 737552,SB-737552,S8510,SB737552,S-8510,S 8510

Cat. No.	Product Name	Target	Signaling Pathways
T26366	Dehydroepiandrosterone sulfate PB 005,PB005,Prasterone sulfate,DHEA sulfate,DHEAS,PB-005	Others	Others
	Dehydroepiandrosterone sulfate (PB-005) 影响神经元的迁移、树突的分枝和新突触的形成。
T14011	2-Arachidonoylglycerol	Cannabinoid Receptor; Endogenous Metabolite	GPCR/G Protein; Metabolism
	2-Arachidonoylglycerol 属于人内源性代谢物，是中枢神经系统中的一种内源性大麻素配体。

天然产物

Dehydroepiandrosterone sulfate

Cat.No: T26366

Synonym: PB 005,PB005,Prasterone sulfate,DHEA sulfate,DHEAS,PB-005

Target: Others

2-Arachidonoylglycerol

Cat.No: T14011

Synonym:

Target: Cannabinoid Receptor, Endogenous Metabolite

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