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.
Products for 5-HT Receptor
- Cat.No. 产品名称 Information
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GC31018
NEO 376 (SPI-376)
SPI-376
NEO 376 (SPI-376) 是 5-HT1 受体、GABA 受体和多巴胺受体的选择性调节剂,具有抗精神病活性。 -
GC32563
Nexopamil racemate
奈索帕米
Nexopamilracemate是Nexopamil的外消旋体。Nexopamil是体内血栓形成和体外血小板聚集中的一种联合Ca2+/5-HT2拮抗剂。
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GC63111
NLX-204 hydrochloride
NLX-204 is a potent, selective agonist of ERK1/2 phosphorylation-preferring serotonin 5 HT1A receptor with pKi of 10.19.
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GC11989
Nortriptyline (hydrochloride)
盐酸去甲替林; Desmethylamitriptyline hydrochloride; Desitriptilina hydrochloride
A tricyclic antidepressant -
GC31015
NRA-0160
NRA-0160是一种选择性的dopamineD4receptor拮抗剂,Ki值为0.48nM;同时对dopamineD2receptor,D3receptor,大鼠5-HT2Areceptor和α1adrenoceptor分别具有不同程度的亲和度,Ki值分别为>10000nM,39nM,180nM和237nM。
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GN10607
Nuciferine
荷叶碱
An alkaloid with diverse biological activities -
GC31173
Ocaperidone (R79598)
奥卡哌酮,R79598
Ocaperidone (R79598) 是一种有效的抗精神病药,作为有效的 5-HT2 和多巴胺 D2 拮抗剂和 5-HT1A 激动剂,对 5-HT2 的 Kis 分别为 0.14 nM、0.46 nM、0.75 nM、1.6 nM 和 5.4 nM 、a1-肾上腺素受体、多巴胺 D2、组胺 H1 和 a2-肾上腺素受体,h5-HT1A 的 pEC50 和 pKi 分别为 7.60 和 8.08。 -
GC12495
Olanzapine
奥氮平; LY170053
Olanzapine是一种单胺拮抗剂。 -
GC61809
Olanzapine D3
奥氮平 D3; LY170053-d3
OlanzapineD3(LY170053D3)是Olanzapine的氘代物。Olanzapine是一种选择性单胺能拮抗剂,高亲和力结合5-羟色胺H1,5HT2A/2C,5HT3,5HT6(Ki分别为7、4、11、57和5nM),多巴胺D1-4(Ki=11-31nM),毒蕈碱M1-5(Ki=1.9-25nM)和肾上腺素α1受体(Ki=19nM)。Olanzapine是一种非典型的抗精神病剂。 -
GC16142
Ondansetron
昂丹司琼; GR 38032; SN 307
A Certified Reference Material -
GC11814
Ondansetron HCl
盐酸昂丹司琼; GR 38032 hydrochloride; SN 307 hydrochloride
A Certified Reference Material -
GC11651
Ondansetron hydrochloride dihydrate
盐酸昂丹司琼二水物; GR 38032 hydrochloride dihydrate; SN 307 hydrochloride dihydrate
An Analytical Reference Material -
GC71604
Ondansetron-d3 hydrochloride
Ondansetron-d3 hydrochloride是氘标记的盐酸昂丹司琼。
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GC71603
Ondansetron-d5
Ondansetron-d5是氘标记的昂丹司琼。
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GC61889
OPC-14523 hydrochloride
OPC-14523盐酸盐
OPC-14523 hydrochloride 是一种具有口服活性的 sigma 和 5-HT1A 受体激动剂,对 sigma 受体 (σ1/2 IC50=47/56 nM)、5-HT1A 受体 (IC50=2.3 nM) 和 5-HT 转运体 (IC50=80 nM) 具有高度亲和力。OPC-14523 hydrochloride 显示抗抑郁药样活性。 -
GC38828
Org-12962
1-[6-氯-5-(三氟甲基)吡啶-2-基]哌嗪
A 5-HT2C receptor agonist -
GC61401
Oxatomide
欧诗美锭
Oxatomide是一种有效的具有口服活性的双重H1组胺受体(H1-histaminereceptor)和P2X7受体拮抗剂,具有抗组胺和抗过敏活性。Oxatomide几乎完全阻断人P2X7受体中ATP诱导的电流(IC50为0.95μM)。Oxatomide可抑制ATP诱导的Ca2+内流,IC50值为0.43μM,并且还抑制5-羟色胺(serotonin)。 -
GC60293
p-MPPI hydrochloride
p-MPPI hydrochloride 是一种选择性的,具有高亲和力的 5-HT1A 受体拮抗剂。p-MPPI hydrochloride 能穿过血脑屏障,具有明显的抗抑郁和抗焦虑作用。
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GC61167
Paliperidone palmitate
棕榈酸帕利哌酮,9-Hydroxyrisperidone palmitate
Paliperidone Palmitate (9-hydroxyrisperidone palmitate) is a palmitate ester of paliperidone, which is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class. -
GC36844
Palonosetron
帕洛诺司琼
Palonosetron (RS25259, RS 25259 197) is a 5-HT3 antagonist with Ki value of 0.17 nM. It is used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV). -
GC17917
Palonosetron HCl
盐酸帕洛诺司琼
A 5-HT3 receptor antagonist -
GC31022
Pancopride (LAS 30451)
泮考必利,LAS 30451
Pancopride (LAS 30451) 是一种新型的强效选择性 5-HT3 受体拮抗剂。 -
GC31069
Pardoprunox (SLV-308)
SLV-308; DU-126891
Pardoprunox hydrochloride (DU-126891, SME-308) is a potent but partial dopamine D2 receptor agonist with pEC50 of 8.0, and a partial agonist in the induction of [35S]GTPγS binding with pEC50 of 9.2 and a serotonin 5-HT1A receptor agonist, with pEC50 of 6.3, respectively. -
GC30980
Pardoprunox hydrochloride (SLV-308 hydrochloride)
盐酸帕多芦诺,SLV-308 hydrochloride; DU-126891 hydrochloride
A dopamine D2 and D3 receptor partial agonist and 5-HT1A agonist -
GC18102
Paroxetine maleate
马来酸帕罗西汀
5-HT uptake inhibitor -
GC31767
Peptide 401
Peptide401是一种有效的来源于蜂毒中的肥大细胞脱颗粒肽,抑制血管通透性。
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GC39237
Perospirone
哌罗匹隆; SM-9018 free base
Perospirone (SM-9018 free base) is an orally active antagonist of 5-hydroxytryptamine2 (5-HT2) receptor, dopamine2 (D2) receptor and 5-HT1A receptor with Ki of 0.6 nM, 1.4 nM and 2.9 nM, respectively. -
GC12293
Perphenazine
奋乃静
A typical antipsychotic -
GC36875
Perphenazine D8 Dihydrochloride
奋乃静 D8 二盐酸盐
Perphenazine D8二盐酸盐是Perphenazine氘代化合物标准品。 -
GC50668
PF 04479745
PF 04479745 是一种有效的选择性 5-HT2C 受体激动剂(EC50:10 nM,ki:15 nM)。 PF 04479745 可用于高血压等心血管疾病的研究。
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GC45791
PF-04995274
A partial 5-HT4 agonist
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GC30953
Phenylbiguanide (N-Phenylbiguanide)
1-苯基双胍,N-Phenylbiguanide; PBG; 1-Phenylbiguanide
1-Phenylbiguanide (Phenylbiguanide, PBG, N-Phenylbiguanide) is a 5-hydroxytryptamine3 (5-HT3) receptor agonist with EC50 of 3.0 μM. -
GC19294
Piboserod
哌波色罗,SB-207266
A selective, potent 5-HT4 receptor antagonist -
GC36912
Piboserod hydrochloride
SB-207266 hydrochloride
Piboserod (SB 207266)盐酸盐是5-羟色胺受体5-HT4选择性抑制剂。 -
GC11844
Pimavanserin
匹莫范色林; ACP-103
A 5-HT2A inverse agonist -
GC36919
Pimavanserin tartrate
匹莫范色林L-酒石酸盐,ACP-103 hemitartrate
A 5-HT2A inverse agonist -
GC30999
Pimethixene (Pimetixene)
匹美噻吨,Pimetixene
Pimethixene (Pimetixene) 是抗组胺药和抗血清素能化合物,用作抗偏头痛剂。 -
GC65296
Pimethixene maleate
匹美噻吨马来酸盐; Pimetixene maleate
Pimethixene (Pimetixene) maleate, an antihistamine, anntimigraine agent and antiserotonergic compound, is a highly potent antagonist of a broad range of monoamine receptors, including a variety of serotonin receptors. Pimethixene maleate inhibits 5-HT2A, 5-HT2B, 5-HT2C, 5-HT1A, 5-HT1B, 5-HT6, 5-HT7, Adrenergic α-1A, Dopamine D1 Receptor, Dopamine D2 Receptor, Dopamine D4.4 Receptor, Histamine H1 Receptor, Muscarinic M1 and Muscarinic M2 with pKi of 10.22, 10.44, 8.42, 7.63, < 5, 7.30, 7.28, 7.61, 6.37, 8.19, 7.54, 10.14, 8.61 and 9.38, respectively. -
GC17734
Pindolol
吲哚洛尔; LB-46
A β1- and β2-AR antagonist -
GC36924
Pipamperone
酰胺哌啶酮,Floropipamide; McN-JR 3345; R 3345
Pipamperone (Floropipamide; McN-JR 3345; R 3345) 是 5-HT2A 受体 (pKi=8.2) 和 D4 受体 (pKi=8.0) 的高亲和力拮抗剂。Pipamperone (Floropipamide; McN-JR 3345; R 3345) 是 D2 受体 (pKi=6.7) 的低亲和力拮抗剂。 -
GC25756
Pirenperone
R-47456, R-50656
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). -
GC13053
Pizotifen
苯噻啶; Pizotyline; BC-105
A triptan -
GC13478
Pizotifen Malate
苯噻啶苹果酸盐,Pizotyline malate; BC-105 malate
A triptan -
GC17854
PNU 142633
PNU 142633 是一种高亲和力、选择性和口服活性的 5-HT1D 受体激动剂,对人 5-HT1D 受体和人 5-HT1B 受体的 Kis 分别为 6 nM 和 \u003e 18 000 nM。
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GC11714
Prucalopride
普芦卡必利
A selective 5-HT4 receptor agonist -
GC13291
Prucalopride Succinat
琥珀酸普芦卡必利; R-108512
A selective 5-HT4 receptor agonist -
GC72789
Pruvanserin
EMD 281014 free acid; LY 2422347
Pruvanserin(EMD 281014游离酸)是一种选择性5-HT2A受体拮抗剂。 -
GC50564
PRX 07034
5-氯-2,3-二甲氧基-Α-甲基-N-[2-(甲基磺酰基)-5-(1-哌嗪基)苯基]-苯甲胺盐酸盐
PRX 07034 是一种高度选择性和有效的 5-HT6 受体拮抗剂,Ki = 4-8 nM,IC50 为 19 nM。 -
GC10450
PRX-08066
A 5-HT2B receptor antagonist
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GC16788
PRX-08066 Maleic acid
5-HT2B receptor antagonist,potent and selective