Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1291 |
Cisapride
西沙必利,西沙比利,Prepulsid,R 51619,Pridesia,Kaudalit,(±)-Cisaprid,Kinestase |
Potassium Channel; 5-HT Receptor; HER | Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Membrane transporter/Ion channel; Neuroscience; Tyrosine Kinase/Adaptors |
Cisapride (R 51619) 是一种5-HT4受体激动剂,还是 hERG 抑制剂。它可作用于肠道中的血清素受体,促进肠道蠕动,增加胃排空并减少食管反流。 | |||
T21946 |
BIMU 8
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
BIMU 8 是 5-HT4 的选择性激动剂,对野生型 5HT4 受体、T3.36A 和 W6.48A 突变体 5-HT4 的 EC50 分别为 18 nM、77 nM 和 540 nM。 | |||
T22671 |
CJ 033466
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
CJ 033466 是 5-HT4 受体 (EC50 = 9 nM) 的特异性部分激动剂,具有促胃动力作用。 | |||
T22992 |
ML 10302 hydrochloride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
ML 10302 hydrochloride 是一种特异性激动剂 5-HT4 并结合 5-HT 受体,5-HT4 和 5-HT3 的 Kis 分别为 1.07 nM 和 782 nM。 | |||
T28934 |
Felcisetrag
TD 8954,TD8954,TD-8954 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Felcisetrag (TD-8954) 是一种有效且选择性的口服活性 5-HT4 受体激动剂,具有胃肠道促动力特性。Felcisetrag 对人类重组 5-HT4(c) (h5-HT4(c)) 受体显示出高亲和力 ,pKi 为9.4。 | |||
T28043L |
Minesapride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Minesapride 是一种新型5-羟色胺4(5-HT4)受体部分激动剂,是一种潜在的胃肠道促动力剂,可用于治疗肠易激综合征伴便秘。 | |||
T6958 |
Prucalopride Succinate
琥珀酸普芦卡必利,R-108512,琥珀酸普卡比利,Resolor Succinate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Prucalopride Succinate (Resolor Succinate) 是5-HT4受体选择高亲和性激动剂,对5-HT4a 和5-HT4b 的 Ki 值分别为 2.5 和 8 nM。 | |||
T27117 |
DA-6886
DA6886,DA 6886 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
DA-6886 是一种 5-羟色胺受体 4(5-HT4)激动剂。DA-6886 以 5-HT4 受体拮抗剂敏感的方式诱导大鼠食道制剂松弛。在表达 hERG 通道的 CHO 细胞中对 DA-6886 进行的评估显示,它抑制 hERG 通道电流的 pIC50 值为 4.3,表明该化合物对 5-HT4 受体的选择性比 hERG 通道高 1000 倍。 | |||
T38507 |
Renzapride
BRL 24924 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Renzapride (BRL 24924) 是一种混合 5-羟色胺 4 型 (5-HT4) 激动剂和 5-HT3 受体拮抗剂。Renzapride 可用于研究以便秘为主的肠易激综合征(C-IBS)。 | |||
T5336 |
Zacopride hydrochloride
|
Potassium Channel; 5-HT Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Zacopride hydrochloride 是5-HT3受体拮抗剂 (Ki:0.38 nM),也是5-HT4受体激动剂 (Ki:373 nM),具有抗焦虑作用。它对精神分裂症具有潜在的研究价值。 | |||
T68035 |
Capeserod
SL-650155,SL-65.0155 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Capeserod 是一种潜在的 5-HT4 receptor(5-羟色胺受体4)激动剂,可用于研究消化系统疾病和神经系统疾病。 | |||
T68116L |
(Rac)-Norcisapride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Norcisapride 是一种5-羟色胺受体3(5-HT3)和(5-羟色胺受体4(5-HT4) 双重激动剂,可用于治疗消化系统疾病、口颌疾病和耳鼻咽喉疾病。 | |||
T21385 |
Cinitapride
西尼必利,Paxapride,Cidine,cinitapride tartrate,Blaston,Cintapro,Cinmove |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Cinitapride (Blaston) 是一种促胃药。它减缓肌肉的活动,以减轻诸如胃酸反流、胃排空延迟和溃疡性消化不良等病症的症状。 Cinitapride 作为 5-HT2 受体的拮抗剂和 5-HT1 和 5-HT4 受体的激动剂。 | |||
T23265 |
RS 67333 hydrochloride
RS 67333 (hydrochloride),RS 67333 HCl,盐酸RS67333 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
RS 67333 hydrochloride (RO5203648) 是一种有效的、选择性的5-HT4 受体 (5-HT4R) 部分激动剂,在豚鼠纹状体中的 pKi 为 8.7。RS 67333 hydrochloride 对其他几种受体的亲和力较低,包括 5-HT1A、5-HT1D、5-HT2A、5-HT2C、多巴胺 D1、D2 和毒蕈碱 M1-M3 受体。RS 67333 hydrochloride 具有神经保护作用,可用于阿尔茨海默病研究。 | |||
T1551 |
Tegaserod maleate
HTF-919,马来酸替加色罗,SDZ-HTF-919 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Tegaserod maleate (SDZ-HTF-919) 是选择性5-HT4受体的部分激动剂和5-HT2B 受体的拮抗剂,用于治疗肠易激综合征和便秘。 | |||
T4616 |
Metoclopramide
甲氧氯普胺,胃复安,5-Chloro-2-methoxyprocainamide |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Metoclopramide (5-Chloro-2-methoxyprocainamide) 是5-HT3和多巴胺D2受体拮抗剂,IC50值分别为 308 和 483 nM,可用于恶心呕吐、胃食管反流和胃轻瘫的研究。 | |||
T2542L |
Prucalopride hydrochloride
Prucalopride HCl |
||
Prucalopride hydrochloride is a selective agonist of the 5-HT4. | |||
T71308 | DSP-6952 | ||
DSP-6952 is a 5-HT4 receptor partial agonist, inhibiting visceral hypersensitivity and ameliorating gastrointestinal dysfunction. | |||
T22294 |
Cinitapride Hydrogen Tartrate
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Cinitapride Hydrogen Tartrate is a gastroprokinetic agent that acts as an antagonist of the 5-HT2 receptors and as an agonist of the 5-HT1 and 5-HT4 receptors | |||
T28696 |
SC 53116 Hydrochloride
SC 53116,SC53116,SC-53116,SC 53116 HCl |
||
SC 53116 Hydrochloride is selective agonist of the newly identified serotonin 5-HT4 receptor subtype. | |||
T22296 |
Cisapride hydrate
Propulsid,Alimix,Enteropride,Kinestase,西沙比利,Propulsin |
EGFR; 5-HT Receptor | Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Neuroscience; Tyrosine Kinase/Adaptors |
Cisapride acts directly as a selective agonist of serotonin 5-HT4 receptor with IC50 value of 0.483 μM. And It also acts indirectly as a parasympathomimetic. | |||
T23791 | BIMU-1 | ||
BIMU-1 is an agonist of 5-HT4 receptor. | |||
T26944 |
Capeserod HCl
SL-65.0155,SL-650155,SL 650155,SL 65.0155 |
||
Capeserod HCl, a 5-hydroxytriptamine 4 (5-HT4) receptor agonist, is used potentially for the treatment of Alzheimer's disease. | |||
T29115 |
VRX 03011 Potassium salt
PRX-03140,PRX3140,NTC942,NTC-942,PRX-3140,PRX03140 |
||
VRX 03011, a 5-HT4 partial agonist, is used potentially for the treatment of Alzheimer's disease. | |||
T27021 |
Cinitapride Tartrate
|
||
Cinitapride Tartrate is an agonist of the 5-HT1 and 5-HT4 receptors and is also an antagonist of the 5-HT2 receptors. | |||
T6597L |
Mosapride citrate dihydrate
GR-107719-B,Mosapride Citrate,GR 107719 B,AS 4370,AS-4370,TAK-370 |
||
Mosapride Citrate is a 5-HT4 receptor agonist used to stimulate gastrointestinal motility via acetylcholine. Mosapride Citrate facilitates acetylcholine release from the enteric cholinergic neurons. | |||
T28517 |
Renzapride hydrochloride
BRL-24924,ATL1251,ATL-1251,Renzapride HCl,AZM-112 |
||
Renzapride is a 5-HT3 antagonist and 5-HT4 agonist. Renzapride also functions as a 5-HT2B antagonist and has some affinity for the 5-HT2A and 5-HT2C receptors. | |||
T34751 |
Usmarapride free base
SUVN-D4010,SUVN-D 4010,SUVN-D-1208045,SUVN-1004028,SUVN D4010,SUVN-D1003019 |
||
SUVN-D4010 is an effective, selective, brain penetrant, and orally active agonist of 5-HT4 receptor partially used to treat Alzheimer's disease and other dementia-related cognitive dysfunction. | |||
T16737 |
Revexepride
|
Others | Others |
Revexepride is a highly selective agonist of the 5-HT4 receptor and a potential inducer of CYP3A4 enzyme. Revexepride is used for the treatment of gastroesophageal reflux disease. | |||
T35046 |
Velusetrag
TD 5108,TD5108,TD-5108 |
||
Velusetrag(TD-5108)is an effective, selective, and highly potent agonist of the 5-HT4 receptor, and being developed for the treatment of gastroparesis, chronic constipation, and irritable bowel syndrome. | |||
T68116 |
norcisapride
|
||
Norcisapride 属于被称为二苯基吡咯的一类有机化合物。Norcisapride 直接作为5-羟色胺5-HT4受体激动剂发挥作用,并间接作为拟副交感神经发挥作用。Norcisapride 是 Cisapride 的代谢产物。 | |||
T72809 |
(S)-Renzapride
(S)-BRL 24924 |
||
(S)-Renzapride ((S)-BRL 24924) 是 Renzapride 的异构体。Renzapride 是一种 5-HT4受体激动剂,Ki 值为 115 nM。Renzapride 还是一种5HT2b 和5HT3受体拮抗剂。Renzapride 可用于便秘型肠易激综合征(C-IBS)的研究。 | |||
T63069 |
Usmarapride
|
||
Usmarapride (SUVN-D4010) 是一种选择性的、口服具有活力的、有效的、具有血脑屏障通透性的 5-HT4 受体部分激动剂,其 EC50 值为 44 nM。Usmarapride (SUVN-D4010) 能够用于研究阿尔茨海默病相关认知缺陷。 | |||
T60787 |
ML 10302
|
||
ML 10302 是5-HT4受体的有效激动剂(Ki = 1.07 nM),通过激活胆碱能通路在小肠和结肠中诱导明显的运动促进,并具有神经疾病的研究潜力。 | |||
T70070 |
Cisapride tartrate
|
||
Cisapride tartrate is chemically related to metoclopramide, but unlike metoclopramide, it does not cross the blood-brain barrier or have antidopaminergic effects. Cisapride is a serotonin-4 (5-HT4) receptor agonist. Cisapride was indicated for the symptomatic treatment of adult patients with nocturnal heartburn due to gastroesophageal reflux disease. The Food and Drug Administration (FDA) in America stopped the marketing of cisapride as of 14th July 2000. They had received at least 341 reports o... |