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Search Results for " electrophysiological "

14

抑制剂 & 化合物

1

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T8357	SB-200646	5-HT Receptor	GPCR/G Protein; Neuroscience
	SB-200646 是 5-HT2B/5-HT2C 受体的选择性强效拮抗剂，对5-HT2B、5-HT2C 和 5-HT2A 的pKi 值分别为 7.5、6.9 和 5.2。它有口服活性，在体内具有电生理和抗焦虑特性。
T2067	NS11394 NS 11394	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	NS11394 是可口服GABAA 的阳性变构调节剂 (PAM)，Ki 值为 0.5 nM。它对GABAA 的选择性依次为 α5、α3、α2 和α1 受体，具有抗炎和抗焦虑活性。
T24885L	Tiaspirone hydrochloride BMY-13859 hydrochloride,Tiaspirone hydrochloride（87691-91-6 Free base)	Dopamine Receptor; 5-HT Receptor	GPCR/G Protein; Neuroscience
	Tiaspirone hydrochloride (BMY-13859 hydrochloride) 具有抗精神病活性。 Tiaspirone hydrochloride 影响大鼠大脑黑质致密带（A9 DA 细胞）和腹侧被盖区（A10 DA 细胞）多巴胺能神经元的电生理活性。
T70540	Pinokalant LOE-908	SARS-CoV; TRP/TRPV Channel	Membrane transporter/Ion channel; Microbiology/Virology
	Pinokalant (LOE-908) 是一种新型非选性阳离子通道抑制剂。Pinokalant 在体内实验中可显著减少皮质梗死体积，可改善缺血半影区的代谢和电生理状态，可减少大鼠大脑中动脉闭塞后急性期磁共振图像上的病变大小。Pinokalant是一种潜在的SARS-CoV-2蛋白酶抑制剂，可用于研究脑卒中。
T61025	GSK-1482160	P2X Receptor	Membrane transporter/Ion channel; Neuroscience
	GSK-1482160是一种CNS-渗透的P2X7受体负变构调节剂，具有口服活性。P2X7受体参与中枢和外周免疫细胞产生促炎细胞因子，因此GSK-1482160具有研究炎症性疾病的潜力。GSK-1482160具有出色的体外效价(在包括人类在内的多种物种的重组和初始P2X7受体的功能和电生理测试中)和交叉靶标选择性。
T0866	Propafenone Rythmol,普罗帕酮,Propafenonum	Potassium Channel; MRP; Sodium Channel	Immunology/Inflammation; Membrane transporter/Ion channel
	Propafenone (Propafenonum) 是钠通道阻滞剂，它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ，具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡，从而抑制食管癌增殖。
T68185	U 66985
	U 66985 is a Platelet-activating factor (PAF) receptor antagonist that inhibit the electrophysiological effects of PAF.
T68399	Pitrazepin
	Pitrazepin is a new GABAA receptor antagonist reported to antagonize electrophysiological effects of GABA
T26751	BBR 2160 BBR-2160,BBR2160
	BBR 2160 is a dihydropyridine derivative belonging to the group of the so-called tiampidine. BBR 2160 has calcium-antagonistic properties in cardiac tissue. Intracellular microelectrodes have been used to characterize the electrophysiological properties o
T32030	GYKI-16638 HCl GYKI 16,638,GYKI16,638,GYKI-16638,GYKI-16,638,GYKI16638,GYKI 16638
	GYKI-16638 is a novel antiarrhythmic agent that demonstrates combined class IB and class III antiarrhythmic properties in human ventricular muscles, similar to the electrophysiological findings after chronic amiodarone treatment. In addition, GYKI 16638 h
T35082	VU6010608 VU-6010608,VU 6010608
	VU6010608 is an effective mGlu7 NAM with excellent CNS permeability and is powerful in electrophysiological studies in blocking long-term enhancement of high-frequency stimuli.
T22423	SB-200646A	5-HT Receptor	GPCR/G Protein; Neuroscience
	SB-200646A 是一个对 5-HT2B/2C 的选择性超过 5-HT2A 的拮抗剂，5-HT2B，5-HT2C 和 5-HT2A 的 pKi 值分别为 7.5、6.9 和 5.2。SB-200646A 具有口服活性，在体内具有电生理和抗焦虑特性。
TP2078	AC 253
	Amylin (AMY3) receptor antagonist. Inhibits andrenomedulin-stimulated cAMP production in vitro. Protects against oligomeric Aβ-induced increase in intracellular Ca2+, activation of PKA, MAPK, Akt and cFOS and cell death in neuronal cell culture. Blocks el
T71000	RO-5328673
	RO-5328673 is a dual NK2/NK3 antagonist. O5328673. [(3)H]RO5328673 bound to a single saturable site on hNK2, hNK3 and gpNK3 with high-affinity. RO5328673 acted as an insurmountable antagonist at both human and guinea-pig NK3 receptors in the [(3)H]IP accumulation assay. In binding kinetic analyses, [(3)H]RO5328673 had fast association and dissociation rates at hNK2 while it had a fast association rate and a remarkably slow dissociation rate at gp and hNK3. In electrophysiological recordings of g...

化合物

Cat.No: T8357

Target: 5-HT Receptor

Cat.No: T2067

Synonym: NS 11394

Target: GABA Receptor

Tiaspirone hydrochloride

Cat.No: T24885L

Synonym: BMY-13859 hydrochloride,Tiaspirone hydrochloride（87691-91-6 Free base)

Target: Dopamine Receptor, 5-HT Receptor

Cat.No: T70540

Synonym: LOE-908

Target: SARS-CoV, TRP/TRPV Channel

Cat.No: T61025

Target: P2X Receptor

Cat.No: T0866

Synonym: Rythmol,普罗帕酮,Propafenonum

Target: Potassium Channel, MRP, Sodium Channel

Cat.No: T68185

Cat.No: T68399

Cat.No: T26751

Synonym: BBR-2160,BBR2160

Cat.No: T32030

Synonym: GYKI 16,638,GYKI16,638,GYKI-16638,GYKI-16,638,GYKI16638,GYKI 16638

Cat.No: T35082

Synonym: VU-6010608,VU 6010608

Cat.No: T22423

Target: 5-HT Receptor

Cat.No: TP2078

Cat.No: T71000

Cat. No.	Product Name	Target	Signaling Pathways
T20636	Latrunculin B LAT-B,LATB,NSC 339663,NSC339663,NSC-339663,LAT B,INS115644	Antifungal	Microbiology/Virology
	Latrunculin B 是一种来自红海海绵的生物碱，是一种肌动蛋白聚合 (actin polymerization) 抑制剂，具有抗真菌和抗原生动物活性。Latrunculin B 调节肺静脉电生理特征并减轻牵张性心律失常的发生，可用于研究青少年青光眼。

天然产物

Cat.No: T20636

Synonym: LAT-B,LATB,NSC 339663,NSC339663,NSC-339663,LAT B,INS115644

Target: Antifungal

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