Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T39429 |
AHN 1-055 hydrochloride
3α-Bis-(4-fluorophenyl) Methoxytropane hydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
AHN 1-055 hydrochloride (3α-Bis-(4-fluorophenyl) Methoxytropane hydrochloride) 与多巴胺转运蛋白具有高亲和力,是多巴胺摄取抑制剂,IC50为 71 nM。 | |||
T8702 |
SKF-83566
|
Dopamine Receptor; 5-HT Receptor; AChR | GPCR/G Protein; Neuroscience |
SKF-83566 是一种具有血脑渗透性和口服活性的 D1 样多巴胺受体拮抗剂和一种较弱的竞争性 5-HT2 受体拮抗剂,Ki 为 11 nM。它是竞争性多巴胺转运蛋白抑制剂,可用于研究帕金森氏症和对尼古丁渴望的缓解的相关研究。 | |||
T1233 |
Oxolinic acid
Emyrenil,Nidantin,NSC 110364,恶喹酸,Dioxacin,Urinox |
Dopamine Receptor; DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Microbiology/Virology; Neuroscience |
Oxolinic acid (Nidantin) 是一种抗生素,对革兰氏阴性菌和革兰氏阳性菌均有效,可研究急性和慢性尿路感染。它是一种 DNA/RNA 合成抑制剂,也是一种多巴胺摄取抑制剂,能刺激小鼠的活跃过度。 | |||
T0031L |
Ziprasidone hydrochloride
盐酸齐拉西酮,齐拉西酮盐酸盐,CP-88059 hydrochloride,CP-88059,Ziprasidone HCl |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ziprasidone hydrochloride (CP-88059 hydrochloride) 是一种联合 5-HT(5-羟色胺)和多巴胺受体拮抗剂,具有抗精神病活性的强效作用。它也是去甲肾上腺素再摄取抑制剂。 | |||
T7341 |
Diclofensine
Ro 8-4650,(+/-)-双氮奋兴 |
Dopamine Receptor; Monoamine Transporter | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Diclofensine (Ro 8-4650) 是一种高效单胺再摄取抑制剂,在大鼠脑突触体中能够阻断多巴胺 (IC50=0.74 nM)、去甲肾上腺素 (IC50=2.3 nM) 和 5-羟色胺 (IC50=3.7 nM)。 | |||
T22508 |
3-CPMT
Chlortropbenzyl hydrochloride,3-[(4-chlorophenyl)-phenylmethoxy]-8-methyl-8-azabicyclo[3.2.1]octane hydrochloride,SL6057,Wy 2149,FC-1 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
3-CPMT (FC-1) 是一种多巴胺摄取抑制剂和一种有效的长效抗组胺剂。 | |||
T19337 |
GBR 12783 dihydrochloride
GBR12783 2HCl |
Others | Others |
GBR 12783 dihydrochloride (GBR12783 2HCl) 是一种特异性,有效且选择性的多巴胺摄取抑制剂,可抑制大鼠和小鼠纹状体突触小体对 [3H] 多巴胺 ([3H]dopamine) 的摄取,IC50值分别为 1.8 nM 和 1.2 nM。GBR 12783 dihydrochloride 还可改善大鼠记忆力并增加海马通路乙酰胆碱的释放。 | |||
T23234 |
Rimcazole dihydrochloride
|
Others | Others |
Rimcazole dihydrochloride 是 Rimcazole 的盐酸盐,是一种σ受体拮抗剂。Rimcazole dihydrochloride 还与多巴胺转运蛋白结合,抑制多巴胺的摄取。 | |||
T7070 |
Nomifensine maleate
Nomifensine (maleate),诺米芬新马来酸盐,(±)-Nomifensine maleat |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Nomifensine maleate (Nomifensine (maleate)) 是一种多巴胺摄取的选择性抑制剂,可用于成人注意力缺陷障碍的研究。 | |||
T1568 |
Amoxapine
阿莫沙平,CL-67772 |
GlyT | Neuroscience |
Amoxapine (CL-67772) 是一种dibenzoxazepine 家族的四环抗抑郁药,常被归类为仲胺三环类抗抑郁药。 | |||
T1336 |
Benztropine mesylate
Benzotropine mesylate,苯扎托品,Benzatropine mesylate,Benztropine methanesulfonate,甲磺酸苯扎托品 |
Dopamine Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Benztropine mesylate (Benztropine methanesulfonate) 是一种可口服的中枢性抗胆碱能剂,用于帕金森氏病的研究。它是抗组胺剂,抑制多巴胺的吸收。它也是人 D2多巴胺受体的变构拮抗剂,具有抗癌症干细胞的作用。 | |||
T41194 |
FFN 102 mesylate
|
Others | Others |
FFN 102 mesylate 是pH 响应型荧光假神经递质(FFN),作为选择性多巴胺转运蛋白(DAT)和VMAT2底物。FFN 102 mesylate 与38个中枢神经系统受体(包括多巴胺和血清素受体)无明显结合。它的Ex-max在pH 值5时为340 nm,在pH 值7.5时为370 nm,在pH 值为5和7.5时,Em-max为435 nm。 | |||
T68070 |
Fezolamine
|
Norepinephrine | Neuroscience |
Fezolamine 是一种新型可口服的非三环类化合物,具有抗抑郁活性。它在体外阻断[3H]去甲肾上腺素的突触体摄取方面的选择性是摄取[4H]3-羟色胺或[3H]多巴胺的3至2倍。在使用单胺耗尽动物的经典行为测试中,它阻止了利血平和四苯的抑制作用。 | |||
T7153 |
Vanoxerine dihydrochloride
GBR-12909 dihydrochloride,伐诺司林二盐酸盐,I893 dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) 是一种竞争性的、有效的、选择性的多巴胺再摄取抑制剂,能够与多巴胺转运体 (DAT) 上的靶点结合。 | |||
T22799 |
GBR 13069 dihydrochloride
|
Others | Others |
GBR 13069 dihydrochloride is a dopamine uptake inhibitor. | |||
T24712 | Rimcazole | ||
Rimcazole is a sigma receptor antagonist. It also binds to the dopamine transporter and inhibiting dopamine uptake. | |||
T71528 |
MCN-5908
|
||
MCN-5908 is a dopamine uptake inhibitor. | |||
T23718 |
Amfonelic Acid
|
||
Amfonelic Acid is a dopamine uptake blocker. | |||
T22877 |
JHW 007 hydrochloride
|
Others | Others |
JHW 007 hydrochloride is a Dopamine uptake inhibitor. | |||
T24645 |
Piroheptine HCl
Piroheptine Hydrochloride,Trimol |
||
Piroheptine HCl is an agent of anticholinergic that acts by inhibiting dopamine uptake and completely preventing loss of striatal dopamine in MPTP-treated mice. | |||
T68727 |
GBR-13119
|
||
GBR-13119 is a dopamine uptake inhibitor. | |||
T68709 |
GBR-13098 dimethanesulfonate
|
||
GBR-13098 dimethanesulfonate is an inhibitor of dopamine uptake. | |||
T11371 |
GBR 12783
|
Others | Others |
GBR 12783 can improve memory performance and increase hippocampal acetylcholine release in rats. GBR 12783 is a specific, potent and selective dopamine uptake inhibitor that inhibits the [3H]dopamine uptake by rat and mice striatal synaptosomes with IC50s of 1.8 nM and 1.2 nM, respectively. | |||
T23781 |
Benzatropine
Akitan,Benztropine,NK 02,Cogentinol,Cogentine |
||
Benzatropine is a centrally active muscarinic antagonist. It also inhibits the uptake of dopamine. It has been used in the symptomatic treatment of Parkinson's Disease. | |||
T28349 |
PD-89211
PD89211 |
||
PD 89211 is a selective dopamine D4 receptor antagonist with high selectivity for the DA D4.2 receptor (> 800-fold) as compared to other hDA receptor subtypes, rat brain serotonin, and adrenergic receptors. In vitro, PD 89211 reverses quinpirole-induced [ | |||
T27689 |
JNJ-7925476 HCl
JNJ-7925476,JNJ7925476,JNJ 7925476 |
||
JNJ-7925476 HCl is a triple monoamine uptake inhibitor. JNJ-7925476 Salt blocks the dopamine transporter (DAT), norepinephrine transporter (NET) and serotonin transporter (SERT) in the central nervous system. The ED(50) values for JNJ-7925476 occupancy of | |||
T37699 |
Org 24598
|
||
Potent and selective inhibitor of the glial glycine transporter GlyT1b (IC50 = 6.9 nM). Displays negligible activity at GlyT-2, adrenoreceptors, dopamine, 5HT receptors and noradrenaline, dopamine, 5HT and GABA transporters (pIC50 in vivo. Chue et al (2013) Glycine reuptake inhibition as a new therapeutic approach in schizophrenia: focus on the glycine transporter 1 (GlyT1). Curr.Pharm.Des. 19 1311 PMID:23194655 |Brown et al (2001) Discovery and SAR of org 24598-a selective glycine uptake inhibi... | |||
T62008 | Mazaticol | ||
Mazaticol 是一种抗胆碱剂,可以阻断毒蕈碱乙酰胆碱受体和胆碱能神经活动。Mazaticol 是有效的 3H-QNB 和 3H-PZ 结合抑制剂,对 M2 受体具有高亲和力。Mazaticol 抑制纹状神经末梢的多巴胺摄取。Mazaticol 在帕金森综合征种有研究价值。 |