Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9420 |
prifinium bromide
|
Others | Others |
Prifinium bromide 是抗胆碱能试剂,能够改善痉挛,具有止吐效果。 | |||
T1460 |
Dicyclomine hydrochloride
|
AChR | Neuroscience |
Dicyclomine hydrochloride 是口服活性毒蕈碱胆碱能受体拮抗剂。它是一种抗痉挛试剂,在体内可缓解胃肠道平滑肌痉挛。它对 M1 受体亚型和 M2 受体亚型,Ki 分别为5.1和54.6nM,在刷状缘膜和基底质膜中均表现出较高的亲和力。 | |||
T5491 |
GSK3179106
|
c-RET | Apoptosis; Tyrosine Kinase/Adaptors |
GSK3179106 是选择性的、具有口服活性的RET 激酶抑制剂,对人和大鼠 RET 的 IC50 分别为 0.4 nM 和 0.2 nM。它能够减轻炎症后和应激引起的内脏超敏反应,对肠易激综合征具有潜在的应用价值。 | |||
T13385 |
Zamifenacin fumarate
扎非那星富马酸盐,UK-76654 fumarate |
AChR | Neuroscience |
Zamifenacin fumarate (UK-76654 fumarate) 是肠道选择性毒蕈碱M3受体的有效拮抗剂, 可显著降低肠易激综合症的结肠蠕动。 | |||
T4691 |
Asimadoline hydrochloride
EMD-61753 hydrochloride,阿西马朵林盐酸盐 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Asimadoline hydrochloride (EMD-61753 hydrochloride) 是一种 κ-阿片(κ-opioid)受体激动剂,对豚鼠和人重组 κ-opioid 的 IC50值分别为 5.6 和 1.2 nM。它可改善糖尿病大鼠的异常性疼痛,具有外周抗炎作用,并有用于肠易激综合征的研究潜力。 | |||
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。 | |||
T4633 |
Asimadoline
EMD-61753,阿西马朵林 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Asimadoline (EMD-61753) 是一种 κ-阿片(κ-opioid)受体激动剂,对豚鼠和人重组 κ-opioid 的IC50值分别为 5.6 和 1.2 nM。它可改善糖尿病大鼠的异常性疼痛,具有外周抗炎作用,并有用于肠易激综合征的研究潜力。 | |||
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。 | |||
T4562L |
Ramosetron hydrochloride
盐酸雷莫司琼,YM 060,YM-060,YM060 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ramosetron hydrochloride (YM-060) 是一种 5-HT3 受体拮抗剂,用于治疗以腹泻为主的肠易激综合征和恶心。 | |||
T22577 |
Antalarmin hydrochloride
|
CRFR; Immunology/Inflammation related | GPCR/G Protein; Immunology/Inflammation |
Antalarmin hydrochloride 是促肾上腺皮质激素释放因子 1 (CRF1) 的拮抗剂。 Antalarmin hydrochloride 具有抗炎作用并抑制与肠易激综合征相关的应激性胃溃疡。 | |||
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)。 | |||
T11852 |
Linaclotide
|
Guanylate cyclase | GPCR/G Protein |
Linaclotide 是一种有效的选择性鸟苷酸环化酶 C 激动剂,可用于治疗便秘型肠易激综合征 (IBS-C) 和慢性便秘的研究。 | |||
T60680 |
Tegaserod
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Tegaserod 是一种可口服的 5-HT4R 激动剂和 5-HT2B 受体拮抗剂,对多种5-羟色胺受体具有抑制作用。 Tegaserod 具有抗肿瘤活性,用于治疗肠易激综合征 (IBS)。 | |||
T12970 |
Solabegron
GW 427353,3'-[[2-[(2R)-2-(3-氯苯基)-2-羟基乙基]氨基]乙基]氨基]-[1,1'-联苯基]-3-羧酸 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Solabegron (GW 427353) 是一种β3肾上腺素能受体 (β3-AR)的选择性激动剂, 在中国仓鼠卵巢细胞中测得 EC50=22 nM,可用于研究膀胱过度活跃和肠易激综合征。 | |||
T69984 |
Ticalopride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ticalopride是一种5-HT3 receptor激动剂,可用于治疗消化系统疾病、口颌疾病、耳鼻咽喉疾病,可用于研究神经性贪食症、胃食管反流和肠易激综合征。 | |||
T0918 |
Trimebutine
曲美布汀,Mebutin |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Trimebutine (Mebutin) 是阿片受体激动剂,有抗毒蕈碱活性。它是解痉剂,可调节肠道和结肠运动,并通过抗毒蕈碱和弱μ-阿片受体激动剂作用缓解腹痛。 | |||
T0786 |
Clidinium bromide
克利溴铵,Ro 2-3773 |
AChR | Neuroscience |
Clidinium bromide (Ro 2-3773) 是季胺抗毒蕈碱剂,可通过减少胃酸和减慢肠道速度,缓解痉挛和腹部疼痛的症状。 | |||
T4562 |
Ramosetron
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ramosetron 是一种血清素 5-HT3 受体拮抗剂,用于治疗恶心和呕吐。它被认为比其他一代 5-HT3 拮抗剂如昂丹司琼具有更高的效力和更长的止吐作用。它还适用于治疗“男性以腹泻为主的肠易激综合征”。它仅获准在日本和选定的东南亚国家使用。 | |||
T30936 |
Cilansetron Hydrochloride
KC-9946,KC9946,KC 9946 |
||
Cilansetron Hydrochloride can be used for irritable Bowel Syndrome (IBS) with Diarrhea Predominance. | |||
T14966 |
Cimetropium Bromide
西托溴铵,DA-3177 |
AChR | Neuroscience |
Cimetropium Bromide is a mAChR antagonist used for long-term treatment of irritable bowel syndrome. | |||
T17283 |
Zamifenacin
UK-76654 |
Others | Others |
Zamifenacin obviously decreases colonic motility in irritable bowel syndrome. Zamifenacin is an effective gut-selective muscarinic M3 receptor antagonist. | |||
T21235 |
Alosetron
Lotronex,GR68755,GR-68755,GR 68755,阿洛司琼 |
||
Alosetron, a 5-HT3 antagonist, is used for the management of severe diarrhea-predominant irritable bowel syndrome (IBS) in women only. | |||
T38482 |
MM 419447
|
||
MM 419447 is a guanylate cyclase-C agonist, and it is a metabolite of linaclotide. This compound, MM 419447, shows promise in the field of irritable bowel syndrome with constipation (IBS-C) research. | |||
T10289 |
Alosetron ((Z)-2-butenedioate)
GR 68755 ((Z)-2-butenedioate),GR 68755X ((Z)-2-butenedioate),马来酸阿洛司琼 |
Others | Others |
Alosetron (GR 68755) (Z)-2-butenedioate is a Serotonin 5HT3-receptor antagonist that is used in the treatment of irritable bowel syndrome. | |||
T16683 |
Pumosetrag Hydrochloride
MKC-733,DDP-733 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pumosetrag Hydrochloride is an orally available 5-HT3 partial agonist. It is developed for the treatment of irritable bowel syndrome and 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. | |||
T11852L |
Linaclotide acetate
MM 416775,MM416775 MD-1100 acetate,Linzess,MM-416775 |
||
Linaclotide acetate is used as an oral guanylate cyclase C agonist linaclotide; 14 amino acid peptide for the potential treatment of constipation-predominant irritable bowel syndrome and chronic idiopathic constipation. | |||
T13002 |
SSR-241586
|
Others | Others |
SSR-241586 is a neurokinin receptors antagonist,and is shown to be active in the treatment of depression, schizophrenia, urinary trouble, emesis, and irritable bowel syndrome (IBS). | |||
T80431 |
δ-Theraphotoxin-Hm1a toxin
|
Sodium Channel | Membrane transporter/Ion channel |
δ-Theraphotoxin-Hm1a毒素是一种针对Nav1.1通道的选择性激活剂,能够诱发疼痛反应和增强触觉敏感度,常用于研究肠易激综合征。 | |||
T64234 | Alosetron (Hydrochloride(1:X)) | ||
Alosetron (GR 68755) Hydrochloride (1:X) 是一种高效的、具有高度选择性的、具有抗炎作用的 5-HT3 受体 (5-HT3 receptor) 拮抗剂。Alosetron Hydrochloride (1:X) 能够阻断 5HT3 介导的豚鼠肌间和粘膜下神经元的快速去极化(IC50:~55 nM)。Alosetron Hydrochloride (1:X) 能够减缓清醒或麻醉犬直肠扩张的内脏伤害性效应。Alosetron Hydrochloride (1:X) 能够用于研究肠易激综合征 (IBS)。 | |||
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。 | |||
T16393 |
ONO-2952
|
Others | Others |
ONO-2952 is more selective for TSPO than other receptors, transporters, ion channels, and enzymes. ONO-2952 is a potent and selective translocator protein 18 kDa (TSPO) antagonist (Ki: 0.33-9.30 nM for rat and human TSPO). ONO-2952 has the potential for i |