5-HT Receptor
5-HT Receptor(5-羟色胺受体)
5-HT receptor (5-hydroxytryptamine receptors) is a group of GPCRs (G protein-coupled receptors) and LGICs (ligand-gated ion channels) found in the central and peripheral nervous systems.
5-HT Receptor 相关产品(419)
- GC25434Frovatriptan SuccinateCAS: 158930-09-7
Frovatriptan Succinate(SB 209509 Succinate,VML 251 Succinate) is the succinate salt form of frovatriptan, a synthetic triptan with serotonin (5-HT) receptor agonist activity especially for the 5-HT1B/1D receptors.
- GC25563Lasmiditan succinateCAS: 439239-92-6
Lasmiditan succinate (COL-144, LY573144) is a novel, centrally acting, highly selective 5-HT(1F) receptor agonist (Ki=2.21 nM) without vasoconstrictor activity.
- GC25569LerisetronCAS: 143257-98-1
Lerisetron (F 0930, F 0930RS) is a 5-HT3 receptor antagonist with IC50 of 0.81μM.
- GC25756PirenperoneCAS: 75444-65-4
Pirenperone (R-47456, R-50656), a quinazoline derivative, is a selective antagonist of SR-2A (5-HT2 serotonin receptor) when employed in low doses. Pirenperone behaves like a typical neuroleptic when used in higher doses (greater than 0.1 mg/kg).
- GC25898SB 200646CAS: 143797-63-1
SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo.
- GC30206Roluperidone (CYR-101)CAS: 359625-79-9纯度: >99.50%
A dual antagonist of 5-HT 2A and σ 2 receptors
- GC30273Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide)CAS: 960151-65-9纯度: >99.50%
Tedatioxetine (Lu AA24530) hydrobromide 可作为 5-HT2A、5-HT2C、5-HT3 和 α;1A-肾上腺素受体拮抗剂,可作为 5-羟色胺和去甲肾上腺素 (NE) 的首选三重再摄取抑制剂 (TRI)。
- GC30280Chlorpromazine D6 hydrochlorideCAS: 1228182-46-4纯度: >99.50%
Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。
- GC30681RevexeprideCAS: 219984-49-3
Revexepride是一种高度选择性的5-HT4receptor激动剂,也是潜在的CYP3A4enzyme诱导剂,可用于治疗胃食管返流疾病。
- GC30796Nelotanserin (APD125)CAS: 839713-36-9纯度: >99.50%
Nelotanserin (APD125) 是一种有效的 5-HT2A 反向激动剂、中度有效的 5-HT2C 部分反向激动剂和弱 5-HT2B 反向激动剂,在 IP 积累试验中 IC50 分别为 1.7、79、791 nM。
- GC30826Temanogrel (APD791)CAS: 887936-68-7纯度: >98.50%
Temanogrel (APD791) 是一种高度选择性的 5-HT2A 受体拮抗剂,Ki 为 4.9 nM。
- GC308888-OH-DPAT (8-Hydroxy-DPAT)CAS: 78950-78-4纯度: >95.00%
8-OH-DPAT 是5-HT1A 激动剂, pIC50 值为 8.19 ,此外8-OH-DPAT对5-HT1B(pIC50 , 5.42)和5-HT (pIC50 <5)受体亲和力都很弱 。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC25434 | Frovatriptan Succinate | 158930-09-7 | - | |
Frovatriptan Succinate(SB 209509 Succinate,VML 251 Succinate) is the succinate salt form of frovatriptan, a synthetic triptan with serotonin (5-HT) receptor agonist activity especially for the 5-HT1B/1D receptors. | ||||
| GC25563 | Lasmiditan succinate | 439239-92-6 | - | |
Lasmiditan succinate (COL-144, LY573144) is a novel, centrally acting, highly selective 5-HT(1F) receptor agonist (Ki=2.21 nM) without vasoconstrictor activity. | ||||
| GC25569 | Lerisetron | 143257-98-1 | - | |
Lerisetron (F 0930, F 0930RS) is a 5-HT3 receptor antagonist with IC50 of 0.81μM. | ||||
| GC25756 | Pirenperone | 75444-65-4 | - | |
Pirenperone (R-47456, R-50656), a quinazoline derivative, is a selective antagonist of SR-2A (5-HT2 serotonin receptor) when employed in low doses. Pirenperone behaves like a typical neuroleptic when used in higher doses (greater than 0.1 mg/kg). | ||||
| GC25898 | SB 200646 | 143797-63-1 | - | |
SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo. | ||||
| GC26002 | Trazodone | 19794-93-5 | >98.00% | |
Trazodone (AF-1161) is a 5-HT 2A/2C receptor antagonist that is used as an antidepressant for treating major depressive disorder and anxiety disorders. | ||||
| GC30198 | Dolasetron Mesylate hydrate | 878143-33-0 | >99.00% | |
A 5-HT 3 receptor antagonist | ||||
| GC30206 | Roluperidone (CYR-101) | 359625-79-9 | >99.50% | |
A dual antagonist of 5-HT 2A and σ 2 receptors | ||||
| GC30273 | Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) | 960151-65-9 | >99.50% | |
Tedatioxetine (Lu AA24530) hydrobromide 可作为 5-HT2A、5-HT2C、5-HT3 和 α;1A-肾上腺素受体拮抗剂,可作为 5-羟色胺和去甲肾上腺素 (NE) 的首选三重再摄取抑制剂 (TRI)。 | ||||
| GC30280 | Chlorpromazine D6 hydrochloride | 1228182-46-4 | >99.50% | |
Chlorpromazine D6 hydrochloride是 Chlorpromazine 的氘代物,可被用于 NMR、GC-MS 或 LC-MS 分析中的内标品,用于定量分析。 | ||||
| GC30314 | 5-HT4 antagonist 1 | 261766-73-8 | - | |
5-HT4antagonist1是一个5-HT4受体拮抗剂,其pKi值为9.6。 | ||||
| GC30352 | Lintopride | 107429-63-0 | - | |
Lintopride是5HT4拮抗剂,对5HT3有轻微拮抗作用。 | ||||
| GC30412 | Dolasetron (MDL-73147) | 115956-12-2 | >98.00% | |
A 5-HT 3 receptor antagonist | ||||
| GC30413 | Dolasetron Mesylate (MDL-73147EF) | 115956-13-3 | - | |
A 5-HT 3 receptor antagonist | ||||
| GC30446 | MHP 133 | 147340-43-0 | - | |
MHP133是一种多靶点抑制剂,可以抑制AChE的活性,KKi值为69μM;同时抑制毒蕈碱M1和M2受体,5HT4受体和咪唑I2受体。 | ||||
| GC30681 | Revexepride | 219984-49-3 | - | |
Revexepride是一种高度选择性的5-HT4receptor激动剂,也是潜在的CYP3A4enzyme诱导剂,可用于治疗胃食管返流疾病。 | ||||
| GC30762 | Harmine (Telepathine) | 442-51-3 | >99.50% | |
A unique regulator of PPARγ expression | ||||
| GC30787 | Sertindole (Lu 23-174) | 106516-24-9 | >99.50% | |
An atypical antipsychotic | ||||
| GC30796 | Nelotanserin (APD125) | 839713-36-9 | >99.50% | |
Nelotanserin (APD125) 是一种有效的 5-HT2A 反向激动剂、中度有效的 5-HT2C 部分反向激动剂和弱 5-HT2B 反向激动剂,在 IP 积累试验中 IC50 分别为 1.7、79、791 nM。 | ||||
| GC30797 | lumateperone Tosylate (ITI-007) | 1187020-80-9 | >99.00% | |
An atypical antipsychotic | ||||
| GC30826 | Temanogrel (APD791) | 887936-68-7 | >98.50% | |
Temanogrel (APD791) 是一种高度选择性的 5-HT2A 受体拮抗剂,Ki 为 4.9 nM。 | ||||
| GC30880 | LP-211 | 1052147-86-0 | >99.50% | |
LP-211是一种选择性的、可透过血脑屏障的5-HT 7 受体(K i =0.58nM)激动剂,选择性高于5-HT 1A 受体(K i =188nM)和D2受体(K i =142nM)。 | ||||
| GC30888 | 8-OH-DPAT (8-Hydroxy-DPAT) | 78950-78-4 | >95.00% | |
8-OH-DPAT 是5-HT1A 激动剂, pIC50 值为 8.19 ,此外8-OH-DPAT对5-HT1B(pIC50 , 5.42)和5-HT (pIC50 <5)受体亲和力都很弱 。 | ||||
| GC30907 | AVN-492 | 1220646-23-0 | >99.50% | |
A 5-HT 6 receptor antagonist | ||||
