Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10169 |
5-HT4 antagonist 1
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT4 antagonist 1 是 5-HT4 的拮抗剂 (pKi = 9.6)。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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)。 | |||
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。 | |||
T15414 |
GR 113808
GR-113808 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
GR 113808 是一种具有选择性的 5-HT4 receptor 拮抗剂,抑制 5-HT1B,5-HT2A,5-HT2C 和 5-HT3 受体,可减弱多巴胺释放。 | |||
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。 | |||
T33940 |
PF-03382792
PF 03382792,PF03382792 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
PF-03382792 是一种小分子 5-HT4 受体激活剂,可用于研究阿尔茨海默病。 | |||
T23310 |
SB-203186 hydrochloride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
SB 203186 hydrochloride 是一种选择性的、竞争性的5-HT4拮抗剂。它拮抗5-HT4受体介导的多巴酚收缩大鼠离体食管弛缓,其在大鼠食管、豚鼠回肠和人类结肠的 pKB 值分别是 10.9、9.5 和 9.0。 | |||
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。 | |||
T13021 |
Sulamserod
RS-100302 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Sulamserod(RS 100302) 是一种有效的 5-HT4 receptor 拮抗剂,具有抗心律失常活性,可用于研究心房颤动和心血管相关疾病。 | |||
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。 | |||
T2278 |
Piboserod
SB-207266,N-[(1-丁基哌啶-4-基)甲基]-3,4-二氢-2H-[1,3]恶嗪并[3,2-a]吲哚-10-甲酰胺 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Piboserod (SB-207266) 是一种5-HT4选择性抑制剂。 | |||
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。 | |||
T4118 |
SB 271046 hydrochloride
SB 271046A |
5-HT Receptor | GPCR/G Protein; Neuroscience |
SB 271046 hydrochloride (SB 271046A) 是高效、选择性和具有口服活性的5-HT6受体拮抗剂,对大鼠、猪和人的pKi 分别为 9.02、8.55 和 8.81。它增加额叶皮层中的细胞外天冬氨酸和谷氨酸并表现出抗惊厥活性,EC50为 0.16 μM。它对 5-HT6 受体、结合位点和离子通道的选择性超过 200 倍。 | |||
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。 | |||
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. | |||
T34407 |
RS 100235
RS100235,RS-100235 |
||
RS 100235 is a 5-HT4 Serotonin Receptor. | |||
T22805 |
GR 125487 sulfamate
|
Others | Others |
GR 125487 sulfamate is a 5-HT4 receptor antagonist. | |||
T11293 |
(±)-Fabesetron hydrochloride
FK1052 hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
FK1052 hydrochloride is a potent 5-HT3 and 5-HT4 receptor dual antagonist. | |||
T2542L |
Prucalopride hydrochloride
Prucalopride HCl |
||
Prucalopride hydrochloride is a selective agonist of the 5-HT4. | |||
T23342 |
SDZ 205-557 hydrochloride
|
Others | Others |
5-HT3/5-HT4 receptor antagonist | |||
T71308 | DSP-6952 | ||
DSP-6952 is a 5-HT4 receptor partial agonist, inhibiting visceral hypersensitivity and ameliorating gastrointestinal dysfunction. | |||
T23260 |
RS 39604
RS 39604 hydrochloride |
Others | Others |
potent and selective 5-HT4 antagonist | |||
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 | |||
T28062 |
ML 10375
ML10375 |
||
ML 10375 is an antagonist of 5-HT4 receptor. | |||
T23255 |
RS 23597-190 hydrochloride
|
Others | Others |
RS 23597-190 hydrochloride is a 5-HT4 receptor antagonist. | |||
T23311 | SB 204070 | Others | Others |
Potent and selective 5-HT4 receptor antagonist | |||
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. | |||
T2278L |
Piboserod hydrochloride
SB 207266 hydrochloride,Piboserod HCl,SB 207266A |
||
Piboserod HCl is a selective antagonist of 5-HT4 and muscarinic receptor. | |||
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. | |||
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. | |||
T28672 |
SB 207710
SB-207710,SB207710 |
||
SB 207710 is a selective and high affinity antagonist of 5-HT4 receptor. | |||
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. | |||
T23791 | BIMU-1 | ||
BIMU-1 is an agonist of 5-HT4 receptor. | |||
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. | |||
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. | |||
T38692 |
Fabesetron
法贝司琼,FK1052 free base |
||
Fabesetron (FK1052) is an orally active compound that acts as a dual antagonist, targeting both the 5-HT3 and 5-HT4 receptors. It exhibits efficacy in studying emesis induced by cancer chemotherapy, showing potential for managing both acute and delayed symptoms. | |||
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。 |