5-HT Receptor
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. Product Name Information
- GC16553 N-Desmethylclozapine 5-HT2C serotonin receptor antagonist
- GC16399 N-Methylquipazine dimaleate 5-HT3 agonist
- GC32511 Naftidrofuryl oxalate (Nafronyl oxalate salt)
- GC31057 Naluzotan (PRX 00023) Naluzotan (PRX 00023) is a novel, potent, and selective amidosulfonamide 5-HT1A agonist with IC50 and Ki of appr 20 nM and 5.1 nM, used for the treatment of anxiety and depression; Also a weak hERG K+ channel blocker, with IC50 of 3800 nM.
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GC15235
NAN-190 hydrobromide
5-HT1A antagonist
- GC11959 Naratriptan Naratriptan is a selective 5-HT1 receptor subtype agonist and is a triptan drug that is used for the treatment of migraine headaches.
- GC36693 Naratriptan D3 Hydrochloride Naratriptan D3 Hydrochloride is the deuterium labeled Naratriptan, which is a selective 5-HT1 receptor subtype agonist.
- GC13298 NAS-181 NAS181 is a potent and selective antagonist of rat 5-HT1B receptor, with a Ki of 47 nM.
- GC13135 NBOH-2C-CN hydrochloride 5-HT2A agonist
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GC69545
Nefazodone
Nefazodone is an orally active phenylpiperazine antidepressant. It effectively and selectively blocks postsynaptic 5-HT2A receptors, moderately inhibits the reuptake of serotonin and noradrenaline. Nefazodone can also alleviate the adverse effects of stress response on the immune system in mice. Nefazodone has a high affinity for CYP3A4 isoenzymes, indicating a potential risk for active molecule-active molecule interactions.
- GC16324 Nefazodone hydrochloride 5-HT2A receptor antagonist
- GC30796 Nelotanserin (APD125) Nelotanserin (APD125) is a potent 5-HT2A inverse agonist, a moderately potent 5-HT2C partial inverse agonist and a weak 5-HT2B inverse agonist, with IC50s of 1.7, 79, 791 nM in IP accumulation assays, respectively.
- GC31018 NEO 376 (SPI-376) NEO 376 (SPI-376) is a selective modulator of 5-HT1 receptor, GABA receptor and dopamine receptor, with anti-psychotic actively.
- GC32563 Nexopamil racemate Nexopamil racemate is the racemate of Nexopamil.
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GC15872
NPEC-caged-serotonin
5-HT receptor agonist
- GC12744 NPS ALX Compound 4a dihydrochloride NPS ALX Compound 4a dihydrochloride is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM.
- GC31015 NRA-0160 NRA-0160 is a selective dopamine D4 receptor antagonist, with a Ki value of 0.48 nM and with negligible affinity for dopamine D2 receptor (Ki: >10000 nM), D3 receptor (Ki: 39 nM), rat 5-HT2A receptor (Ki: 180 nM) and rat α1 adrenoceptor (Ki: 237 nM).
- GC31173 Ocaperidone (R79598) Ocaperidone (R79598) is an effective antipsychotic agent, acting as a potent 5-HT2 and dopamine D2 antagonist, and a 5-HT1A agonist, with Kis of 0.14 nM, 0.46 nM, 0.75 nM, 1.6 nM and 5.4 nM for 5-HT2, a1-adrenergic receptor, dopamine D2, histamine H1 and a2-adrenergic receptor, respectively, and a pEC50 and pKi of 7.60 and 8.08 for h5-HT1A.
- GC12495 Olanzapine Olanzapine (LY170053) is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptor (Ki=19 nM).
- GC16142 Ondansetron serotonin 5-HT3 receptor antagonist
- GC11814 Ondansetron HCl Ondansetron HCl (GR 38032 hydrochloride; SN 307 hydrochloride) is a serotonin 5-HT3 receptor antagonist used mainly as anantiemetic (to treat nausea and vomiting), often following chemotherapy.
- GC11651 Ondansetron hydrochloride dihydrate 5-HT3 receptor antagonist
- GC15268 Org 12962 hydrochloride 5-HT2C receptor agonist
- GC11338 Org 37684 5-HT2 receptors agonist
- GC38828 Org-12962 Org-12962 is a potent, selective and orally active 5-HT2C?receptor agonist with a pEC50?value of 7.01.
- GC36844 Palonosetron Palonosetron is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV).
- GC17917 Palonosetron HCl Palonosetron HCl is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV).
- GC31022 Pancopride (LAS 30451) Pancopride (LAS 30451) is a new potent and selective 5-HT3 receptor antagonist.
- GC31069 Pardoprunox (SLV-308) Pardoprunox (SLV-308) (SLV-308) is a partial dopamine D2 and D3 receptor partial agonist and a serotonin 5-HT1A receptor agonist, with pEC50s of 8, 9.2, and 6.3, respectively.
- GC30980 Pardoprunox hydrochloride (SLV-308 hydrochloride) Pardoprunox (SLV-308) hydrochloride is a partial dopamine D2 and D3 receptor partial agonist and a serotonin 5-HT1A receptor agonist, with pEC50s of 8, 9.2, and 6.3, respectively.
- GC31767 Peptide 401 Peptide 401, a potent mast cell degranulating factor from bee venom, suppresses the increased vascular permeability due to intradermal injection of various smooth muscle spasmogens (histamine, and 5-HT).
- GC12293 Perphenazine dopamine antagonist
- GC36875 Perphenazine D8 Dihydrochloride Perphenazine D8 Dihydrochloride is the deuterium labeled Perphenazine, which is a typical antipsychotic drug(5-HT, Dopamine receptor ligand).
- GC45791 PF-04995274 A partial 5-HT4 agonist
- GC30953 Phenylbiguanide (N-Phenylbiguanide) Phenylbiguanide (N-Phenylbiguanide) is a 5-HT3 receptor selective agonist with an EC50 of 3.0±0.1 μM.
- GC19294 Piboserod Piboserod (SB 207266) is a selective 5-HT(4) receptor antagonist.
- GC36912 Piboserod hydrochloride Piboserod (SB 207266) Hcl is a selective 5-HT(4) receptor antagonist.
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GC11844
Pimavanserin
5-HT2A inverse agonist
- GC36919 Pimavanserin tartrate Pimavanserin (ACP-103) hemitartrate is a potent 5-HT 2A receptor inverse agonist with pIC50 and pKi of 8.73 and 9.3, respectively.
- GC30999 Pimethixene (Pimetixene) Pimethixene (Pimetixene) is antihistamine and antiserotonergic compound, acts as an antimigraine agent.
- GC65296 Pimethixene maleate Pimethixene maleate is antihistamine and antiserotonergic compound, acts as an antimigraine agent.
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GC17734
Pindolol
β-adrenoceptor antagonist with partial agonist activity
- GC36924 Pipamperone Pipamperone (Floropipamide; McN-JR 3345; R 3345) is a high-affinity antagonist of 5-HT2A receptor (pKi=8.2) and D4 receptor (pKi=8.0) and a low-affinity antagonist of D2 receptor (pKi=6.7).
- GC25756 Pirenperone 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 Highly selective 5-HT receptor blocking agent
- GC13478 Pizotifen Malate 5-HT receptor antagonist
- GC15011 PNU 109291 5-HT1D receptor agonist
- GC17854 PNU 142633 5-HT1D receptor agonist
- GC17714 PNU 22394 hydrochloride 5-HT2C agonist and partial 5-HT2A/5-HT2B agonist
- GC11714 Prucalopride 5-HT4A and 5-HT4B receptor agonist
- GC13291 Prucalopride Succinat Prucalopride Succinat is a selective, high affinity 5-HT4 receptor agonist with pKi of 8.6/8.1 for 5-HT4a/4b.
- GC10450 PRX-08066 5-HT2BR antagonist
- GC16788 PRX-08066 Maleic acid 5-HT2B receptor antagonist,potent and selective
- GC32595 PRX933 hydrochloride (GW876167 hydrochloride) PRX933 hydrochloride (GW876167 hydrochloride) is a 5-HT2c receptor agonist extracted from patent WO 2014140631 A1.
- GC17857 PU 02 negative allosteric modulator of 5-HT3 receptors
- GC31393 Pumosetrag Hydrochloride (MKC-733) Pumosetrag Hydrochloride (MKC-733) (MKC-733; DDP-733) is an orally available 5-HT3 partial agonist developed for the treatment of irritable bowel syndrome and gastroesophageal reflux disease.
- GC37055 Quetiapine D4 fumarate Quetiapine D4 fumarate is the deuterium labeled Quetiapine fumarate.
- GC16891 Quetiapine Fumarate Quetiapine Fumarate is a 5-HT receptors agonist with a pEC50 of 4.77 for human 5-HT1A receptor.
- GC16506 Quipazine dimaleate 5-HT3 receptor agonist
- GC13369 R 1485 dihydrochloride 5-HT6 antagonist,selective and high affinity
- GC14583 R 59-022 Diacylglycerol (DAG) kinase inhibitor
- GC17706 R-96544 hydrochloride 5-HT2 receptor antagonist
- GC15639 Ramosetron Hydrochloride 5-HT3 receptor antagonist
- GC67923 Renzapride
- GC64423 Repinotan hydrochloride Repinotan hydrochloride (BAY x 3702) is a potent, selective, brain-penetrant and orally active 5-HT1A receptor agonist, with Ki values of 0.19 nM (calf hippocampus), 0.25 nM (rat and human cortex), and 0.59 nM (rat hippocampus Repinotan hydrochloride has a weak affinity for other related receptors.
- GC30681 Revexepride Revexepride is a highly selective 5-HT4 receptor agonist, and a potential inducer of CYP3A4 enzyme, used for the treatment of gastroesophageal reflux disease.
- GC34158 RG-12915 RG-12915 is a selective 5-HT3 antagonist, with IC50 value of 0.16 nM.
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GC12986
Risperidone
SR-2A inhibitor
- GC37539 Risperidone hydrochloride Risperidone hydrochloride (R 64 766 hydrochloride) 5-HT2 receptor blocker, P-Glycoprotein inhibitor and potent dopamine D2 receptor antagonist, with Kis of 4.8, 5.9 nM for 5-HT2A and dopamine D2 receptor, respectively.
- GC37540 Risperidone mesylate Risperidone mesylate(R 64 766 mesylate) is a serotonin 5-HT2 receptor blocker, P-Glycoprotein inhibitor and potent dopamine D2 receptor antagonist, with Kis of 4.8, 5.9 nM for 5-HT2A and dopamine D2 receptor, respectively.
- GC13883 Ritanserin long-acting 5-HT2 receptor antagonist
- GC10460 Rizatriptan Benzoate 5-HT Receptor agonist
- GC17260 Ro 04-6790 5-HT6 receptor antagonist
- GC15135 Ro 60-0175 fumarate 5-HT2 receptor agonist
- GC64606 Ro60-0175 Ro60-0175 is a potent and selective agonist of 5-HT2C receptor.
- GC63842 Rodatristat Rodatristat (KAR5417) is a potent tryptophan hydroxylase 1 (TPH1) and TPH2 inhibitor with IC50s value of 33 nM and 7 nM, respectively, and shows robust reduction of intestinal serotonin (5-HT) levels in mice.
- GC30206 Roluperidone (CYR-101) Roluperidone (CYR-101) (CYR-101) is a novel cyclic amide derivative that has high equipotent affinities for 5-HT2A and sigma-2 receptors (Ki of 7.53 nM and 8.19 nM for 5-HT2A and sigma-2, respectively).
- GC14657 Rotundine Dopamine D1 receptor antagonist,potent and selective
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GC15979
RS 16566 dihydrochloride
ligand for the (R)-zacopride binding site
- GC16861 RS 23597-190 hydrochloride 5-HT4 receptor antagonist
- GC14625 RS 39604 hydrochloride RS 39604 hydrochloride is a potent, selective, and orally active 5-HT4 receptor antagonist with a pKi of 9.1 in guinea pig striatal membranes.
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GC15137
RS 56812 hydrochloride
5-HT3 partial agonist
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GC12340
RS 67333 hydrochloride
potent and highly selective 5-HT4 partial agonist
- GC14696 RS 67506 hydrochloride potent and selective 5-HT4 partial agonist
- GC37569 RU 24969 RU 24969 is a preferential 5-HT1B agonist, with a Ki of 0.38 nM, but also displays appreciable affinity for the 5-HT1A receptor (Ki=2.5 nM), and has low affinity for other receptor sites in the brain.
- GC31827 Rupatadine (UR-12592) Rupatadine (UR-12592) (UR-12592) is a potent, orally active and long-lasting dual PAF/H1 antagonist, with Kis of 0.55 μM and 0.1 μM, respectively.
- GC11033 Rupatadine Fumarate Inhibitor of PAF and histamine (H1) receptor
- GC10535 S 32212 hydrochloride inverse agonist of 5-HT2C receptors
- GC64530 Sarizotan Sarizotan (EMD 128130) is an orally active serotonin 5-HT1A receptor and dopamine receptor agonist.
- GC16202 Sarpogrelate hydrochloride 5-HT2A receptor inhibitor
- GC25898 SB 200646 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.
- GC14052 SB 200646 hydrochloride 5-HT2C/2B receptor antagonist
- GC16439 SB 203186 hydrochloride Potent 5-HT4 receptor antagonist
- GC10401 SB 204070 Potent and selective 5-HT4 receptor antagonist
- GC12803 SB 204741 5-HT2B receptor antagonist
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GC10310
SB 206553 hydrochloride
5-HT2B/5-HT2C receptor antagonist
- GC15551 SB 216641 hydrochloride h5-HT1B antagonist
- GC16556 SB 221284 5-HT2C/2B receptor antagonist
- GC13438 SB 224289 hydrochloride 5-HT1B receptor antagonist
- GC14347 SB 228357 5-HT2C/2B receptor antagonist