Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10006 |
5-HT3-In-1
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT3-In-1 (compound example 8) exhabits with 5-HT3 inhibition activity. | |||
T9846 |
5-HT3 antagonist 5
|
||
5-HT3 antagonist 5 是喹喔啉 -2- 甲酰胺化合物,是一种5-HT3受体拮抗剂。5-HT3 antagonist 5 对5-HT3激动剂和2-甲基-5-HT 也具有拮抗作用,并在小鼠中表现出抗抑郁作用。 | |||
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。 | |||
T67956 |
Litoxetine
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Litoxetine 是一种选择性的5-HT 摄取抑制剂,是具有5-HT3受体拮抗剂。Litoxetine 可作为一种抗抑郁剂,在雪貂身上显示出止吐特性。Litoxetine (1和10毫克/公斤静脉注射)剂量依赖性地减少了反胃和呕吐的次数,延迟了呕吐的发生。Litoxetine 对大脑5HT3受体有亲和力(Ki = 85 nM)。 | |||
T4978 |
Sarpogrelate hydrochloride
盐酸沙格雷酯,MCI-9042 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Sarpogrelate hydrochloride (MCI-9042) 是一种选择性5-HT2R 拮抗剂,可用于研究与血栓形成有关的血管疾病,对 5-HT2A、5-HT2B 和 5-HT2C 受体的pKi 值分别为 8.52、6.57 和 7.43。 | |||
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)。 | |||
T75954 |
Mambalgin 1 TFA
|
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Mambalgin 1 TFA, a selective inhibitor of ASIC1a (with IC50 values of 192 nM for human ASIC1a and 72 nM for the ASIC1a/1b dimer), preferentially binds to the channel in its closed/inactive state. It demonstrates selectivity for ASIC1a over a range of other channels, including ASIC2a, ASIC3, TRPV1, P2X2, 5-HT3, Nav1.8, Cav3.2, and Kv1.2. In vivo, Mambalgin 1 TFA effectively prolongs the latency of the withdrawal response in mouse tail-flick and paw-flick tests. |