Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T24055 |
FAUC 213
FAUC213,FAUC-213 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
FAUC 213 是一种具有口服活性的‘、高度选择性的、可透过血脑屏障的多巴胺 D4受体完全拮抗剂,对 hD4.4的 Ki=2.2 nM。它对 D2和 D3受体的活性较低,对于 hD2、hD3的 Ki 分别为 3.4 μM、5.3 μM。它表现出非典型的抗精神病活性。 | |||
T1684 |
Nitisinone
尼替西农,NTBC,SC0735,Nitisone |
Others; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB; Others |
Nitisinone (SC0735) 是一种 4-羟基苯丙酮酸双加氧酶抑制剂。 | |||
T37197 |
5-HT1A modulator 2 hydrochloride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
5-HT1A modulator 2 hydrochloride 是 8-OH-DPAT 的一种衍生物,是5-HT1A 的调节剂,Ki 为 53 nM。 | |||
T10168 |
5-HT1A modulator 1
5-HT1Amodulator1 |
Phospholipase; Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
5-HT1A modulator 1 对 5-HT1A、α1-肾上腺素能受体和 D2 受体具有非常高的亲和力(IC50s = 2 nM、10 nM 和 40 nM)。 | |||
T62843 | 5-HT1A antagonist 1 | ||
5-HT1A antagonist 1 (compound 6f) 是一种有效的、选择性的 5-HT1Areceptor 受体拮抗剂 (Ki: 35 nM)。5-HT1A antagonist 1 能够用于研究中枢神经系统疾病。 | |||
T27558 |
HT1042
HT 1042,HT-1042 |
||
HT1042 is an inhibitor of the β5i component of the 20S proteasome complex, it is used to aid in the treatment of inflammatory diseases, autoimmune and hematologic malignancies. | |||
T10872L |
CP 96021
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
CP 96021是一组5-HT1受体和5-HT2受体拮抗剂,具有抗炎特性,是治疗胃肠道和呼吸道哮喘的非自身抗溃疡化合物。 | |||
T12207 |
NEO 376
SPI-376 |
Dopamine Receptor; 5-HT Receptor; GABA Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
NEO 376 (SPI-376) 是选择性5-HT1 受体、GABA 受体和多巴胺受体调节剂,可用于精神病的研究。 | |||
T8666 |
Naratriptan
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Naratriptan 是一种5-HT1受体选择性激动剂,可作用于偏头疼。 | |||
T0203 |
Sumatriptan succinate
舒马普坦琥珀酸盐,GR 43175,琥珀酸舒马曲坦 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Sumatriptan succinate (GR 43175) 是一种5-HT1受体激动剂,可作用于偏头疼的急性治疗。 | |||
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。 | |||
T22534 |
8-Hydroxy-DPAT hydrobromide
7-(二丙基氨基)-5,6,7,8-四氢-1-萘酚氢溴酸盐,8-OH-DPAT hydrobromide |
5-HT Receptor | GPCR/G Protein; Neuroscience |
8-Hydroxy-DPAT hydrobromide (8-OH-DPAT hydrobromide) 是一种选择性5-HT1A 激动剂,pIC50为 8.19。它对 5-HT1结合位点的亚型有近 1000 倍的选择性。 | |||
T23382 |
Spiroxatrine
R 5188 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Spiroxatrine (R 5188) 是一种选择性和有效性的 5-HT1α 和 α2-adrenergic 双重拮抗剂,具有镇静活性,对5-HT1α、5-HT1 β、5-HT2和多巴胺受体具有抑制作用。Spiroxatrine 可用于研究心血管系统相关疾病。 | |||
T1512 |
Rizatriptan benzoate
苯甲酸利扎曲坦,MK-462 Benzoate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Rizatriptan benzoate (MK-462 Benzoate) 是 5-HT1激动剂,通过选择性结合并激活血清素 (5-HT) 1B 受体和 5-HT 1D 受体,从而缓解偏头痛。 | |||
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。 | |||
T6602 |
Naratriptan hydrochloride
Naratriptan HCl,Amerge,Naramig,盐酸那拉曲坦,GR-85548A hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Naratriptan hydrochloride (GR-85548A hydrochloride) 是一种5-HT1受体激动剂,有抗偏头疼特性。它还可以通过刺激三叉神经系统感觉神经末梢上的 5-HT1D/1B 受体来发挥其作用,从而减少促炎神经肽的释放。 | |||
T0162 |
Quetiapine
ICI204636,Quetiapin,喹硫平 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Quetiapine (ICI204636) 是5-HT 受体激动剂和多巴胺受体拮抗剂,对人5-HT1A 的 pEC50值为 4.77,对人 D2的 pIC50值为 6.33。它用于治疗精神分裂症,以及治疗与 I 型双相情感障碍相关的急性躁狂发作。它对人 D2、HT1、5-HT2A、5-HT2C 受体具有中高等亲和力,pKi 值为 7.25、5.74、7.54和5.55。 | |||
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. | |||
T12176 |
Naratriptan D3 Hydrochloride
GR-85548A D3 |
Others | Others |
Naratriptan D3 Hydrochloride is the deuterium labeled Naratriptan, is a selective agonist of 5-HT1 receptor subtype. | |||
T60989 |
Sumatriptan hydrochloride
|
||
Sumatriptan (GR 43175) hydrochloride 可用于研究偏头痛,它是一种口服有效的5-HT1受体激动剂。Sumatriptan hydrochloride 对5-HT1D、5-HT1B 和5-HT1A 受体的 Ki 值分别为 17 nM、27 nM 和 100 nM。 | |||
T70257 |
Avitriptan HCl
|
||
Avitriptan, also known as BMS-180048, is a selective 5-HT1-like receptor agonist. Avitriptan is an effective compound for the treatment of migraine headaches with a prolonged duration of response. Avitriptan Is a Ligand and Agonist of Human Aryl Hydrocarbon Receptor That Induces CYP1A1 in Hepatic and Intestinal Cells. | |||
T23405 |
Sumatriptan
|
Others | Others |
Sumatriptan succinate is a selective 5-HT1 receptor agonist with specificity towards 5-HT1D, 5-HT1B, and 5-HT1A. | |||
T4375 |
Methiothepin maleate
Metitepine,甲替平 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Methiothepin maleate (Metitepine) 是一种 5-HT1、5-HT6、5-HT7 血清素受体拮抗剂,可阻断血清素自身受体。 | |||
T68176 |
Isamoltane
|
||
Isamoltane is a serotonin 5-HT1 Receptor Antagonist | |||
T22959 |
m-Chlorophenylbiguanide hydrochloride
1-(3-Chlorophenyl)biguanidehydrochloride,1-(3-氯苯基)双胍 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
m-Chlorophenylbiguanide hydrochloride 是一种 5-HT3 受体激动剂。它选择性结合 5-HT3(Ki: 0.002 µM) 超过 5-HT1A(Ki: 10 µM) 和 5-HT2(Ki: 10 µM) 受体,但也结合多巴胺转运蛋白上的高亲和力和低亲和力位点( DAT;IC50:在大鼠尾状壳核突触体膜中分别为 0.4 和 34.8 µM)。 | |||
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 | |||
T78184 |
MMV009085
|
||
MMV009085是一种针对恶性疟原虫己糖转运体PfHT1的特异性抑制剂,具有潜在的抗疟效果。它同时抑制人葡萄糖转运蛋白,强效抑制葡萄糖吸收(IC50:2.6 μM)及恶性疟原虫3D7株的生长(EC50:1.23±0.04 μM)。 | |||
T8136 |
Perospirone hydrochloride
Perospirone HCl,盐酸哌罗匹隆,SM-9018 hydrochloride |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Perospirone hydrochloride (Perospirone HCl) 是非典型的抗精神病剂,可用于精神分裂症的研究。它是可口服的5-HT2A 受体和多巴胺 D2受体的拮抗剂,也是5-HT1A 受体的部分激动剂。 | |||
T12480 |
Pipamperone
Floropipamide,McN-JR 3345,酰胺哌啶酮,R 3345 |
Others; Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
Pipamperone (McN-JR 3345) 是5-HT2A 受体和D4受体的高亲和力拮抗剂,也是D2受体的低亲和力拮抗剂,pKi 分别为 8.2、8.0 和 6.7。 | |||
T38145 | Eltoprazine | ||
Eltoprazine(DU28853) is a serenic or antiaggressive agent which as an agonist at the 5-HT1A and 5-HT1B receptors and as an antagonist at the 5-HT2C receptor.IC50 value:Target: 5-HT1A/1B agonist; 5-HT2C antagonistin vitro: The binding of [3H]eltoprazine to whole tissue sections was saturable and revealed an apparent dissociation constant (Kd) of 11 nM. Specific [3H]eltoprazine binding was completely displaced by 5-HT; conversely, unlabelled eltoprazine reduced [3H]5-HT binding to the levels of no... |