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Inhibitors
| Cat.No. | Name | Information |
|---|---|---|
| M10054 | Paroxetine | Paroxetine is a inhibitor of serotonin uptake. |
| M9763 | AVN-492 | AVN-492 is a potent and selective 5-HT6R antagonist, binds to 5-HT6R (Ki = 91 pM). |
| M9584 | SAM-315 | SAM-31 (WAY-255315) is selective 5-Hydroxytryptamine-6 antagonists. |
| M9565 | RU 24969 hemisuccinate | RU 24969 hemisuccinate is a selective agonist at the 5-HT1A and 5-HT1B receptors. |
| M9308 | LY344864 | LY344864 is a selective 5-HT1F receptor agonist with an affinity of 6 nM (Ki). |
| M9252 | YL-0919 | YL-0919 is a novel 5-HT1A receptor agonist and selective serotonin reuptake inhibitor. |
| M9181 | 8-OH-DPAT | 8-OH-DPAT (8-Hydroxy-DPAT) is a potent and selective 5-HT agonist, with a pIC50 of 8.19 for 5-HT1A. |
| M9025 | Idalopirdine hydrochloride | Idalopirdine hydrochloride is a potent and selective 5-HT6 receptor antagonist with a Ki value of 0.83 nM. |
| M9011 | PRX-08066 | PRX-08066 is a a novel 5-hydroxytryptamine receptor 2B antagonist with IC50 of 3.4 nM. |
| M8955 | MIN-101 | MIN-101 (Roluperidone) is a novel compound with affinities for 5-HT2A and sigma-2 receptors with Ki values of 7.53 nM and 8.19 nM, respectively. |
| M8942 | GSK163090 | GSK163090 is a potent, selective, and orally active 5-HT1A/B/D receptor antagonist. |
| M8932 | Eptapirone | Eptapirone (F11440) is a potent 5HT(1A) receptor agonist with marked anxiolytic and antidepressant potential. |
| M8900 | TG6-10-1 | TG6-10-1 is a potent and selective antagonist for the prostaglandin E2 receptor subtype EP2. |
| M8856 | WAY-100135 dihydrochloride | WAY-100135 dihydrochloride is a potent, selective 5-HT1A receptor antagonist (IC50 = 15 nM). |
| M8033 | Paroxetine hydrochloride hemihydrate | Paroxetine hydrochloride hemihydrate is one of the most potent and selective of the selective serotonin reuptake inhibitors (SSRI); antidepressant. |
| M7684 | Clozapine N-oxide | Clozapine N-oxide (CNO) is a 5-HT2 serotonin receptor antagonist; major metabolite of clopazine that can be monitored by HPLC. |
| M7102 | Paroxetine maleate | Paroxetine maleate is a highly potent and selective 5-HT uptake inhibitor. |
| M6946 | Melperone hydrochloride | Melperone hydrochloride is a 5-HT2A/D2 receptor antagonist; neuroleptic. |
| M6933 | LY334370 | LY 334370 is a selective 5-HT1F agonist. |
| M6065 | Ziprasidone HCl monohydrate | Ziprasidone(CP88059) is a combined 5-HT (serotonin) and dopamine receptor antagonist which exhibits potent effects of antipsychotic activity. |
| M6064 | Ziprasidone HCl | Ziprasidone HCl is a novel and potent dopamine and serotonin (5-HT) receptor antagonist, used in the treatment of schizophrenia and bipolar disorder. |
| M6058 | Vortioxetine | Vortioxetine (Lu AA21004) is a multimodal serotonergic agent, inhibits 5-HT1A, 5-HT1B, 5-HT3A, 5-HT7 receptor and SERT with IC50 of 15 nM, 33 nM, 3.7 nM, 19 nM and 1.6 nM, respectively. |
| M6051 | Venlafaxine | Venlafaxine is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI) class. |
| M6050 | Venlafaxine HCl | Venlafaxine HCl is an arylalkanolamine serotonin-norepinephrine reuptake inhibitor (SNRI), used to treat major depressive disorder (MDD), generalised anxiety disorder (GAD), panic disorder and social phobia. |
| M6027 | Trazodone | Trazodone HCl is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors for treatment of anxiety disorders. |
| M5992 | Tegaserod maleate | Tegaserod maleate is a partial agonist of the 5-HT4 receptor; stimulates the peristaltic reflex and accelerates gastrointestinal transit. |
| M5989 | Tandospirone | Tandospirone(SM-3997) is a potent and selective 5-HT1A receptor partial agonist (Ki = 27 nM) that displays selectivity over SR-2, SR-1C, α1, α2, D1 and D2 receptors (Ki values ranging from 1300-41000 nM). |
| M5951 | Sarpogrelate HCl | Sarpogrelate(MCI-9042) hydrochloride, a selective 5-HT2 antagonist, has been widely used as an anti-platelet agent for the treatment of PAD. |
| M5938 | Rizatriptan Benzoate | Rizatriptan Benzoate is an agonist at serotonin 5-HT1B and 5-HT1D receptors, used to treat acute migraine attacks. |
| M5935 | Risperidone | Risperidone is a mutil-targeted antagonist for dopamine, serotonin, adrenergic and histamine receptors, used to treat schizophrenia and bipolar disorder. |
| M5920 | Ramosetron HCl | Ramosetron Hydrochloride(YM060 Hydrochloride) is a serotonin 5-HT3 receptor antagonist for the treatment of nausea and vomiting. |
| M5884 | Pizotifen | Pizotifen(Pizotyline) is a highly selective 5-HT receptor blocking agent, which is a benzocycloheptane based drug. |
| M5861 | Paroxetine HCl | Paroxetine HCl is an antidepressant compound of the SSRI type. |
| M5835 | Ondansetron Hydrochloride Dihydrate | Ondansetron is a highly specific and selective serotonin 5-HT3 receptor antagonist (Ki=6.16 nM), with low affinity for dopamine receptors. |
| M5804 | Naftidrofuryl oxalate | Naftidrofuryl is a drug used in the management of peripheral and cerebral vascular disorders as a vasodilator, enhance cellular oxidative capacity, and may also be a 5-HT2 receptor antagonist. |
| M5799 | Mosapride Citrate | Mosapride Citrate is a gastroprokinetic agent that acts as a selective 5HT4 agonist. |
| M5798 | Mosapride | Mosapride is a gastroprokinetic agent that acts as a selective 5HT4 agonist. |
| M5754 | Loxapine | Loxapine Succinate is a D2DR and D4DR inhibitor, serotonergic receptor antagonist and also a dibenzoxazepine anti-psychotic agent. |
| M5660 | Fluvoxamine maleate | Fluvoxamine Maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI), used in the treatment of obsessive-compulsive disorder. |
| M5548 | Dalasetron Mesylate hydrate | Dolasetron(MDL-73147) is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy. |
| M5543 | Cyproheptadine hydrochloride sesquihydrate | Cyproheptadine hydrochloride sesquihydrate is an antihistamine and is an antagonist of serotonin and histamine2. |
| M5542 | Cyproheptadine HCl | Cyproheptadine is a histamine receptor antagonist for 5-HT2 receptor with IC50 of 0.6 nM. |
| M5475 | Cabergoline | Cabergoline, an ergot derivative, is a potent dopamine receptor agonist on D2 receptors. |
| M5466 | Blonanserin | Blonanserin is a relatively selective serotonin (5-HT)2A and dopamine D2 antagonist, used the treatment of schizophrenia. |
| M5424 | Asenapine maleate | Asenapine maleate is a high-affinity antagonist of serotonin, norepinephrine, dopamine and histamine receptors, used for the treatment of schizophrenia and acute mania associated with bipolar disorder. |
| M5423 | Asenapine | Asenapine(Org 5222) inhibits adrenergic receptor (α1, α2A, α2B, α2C) with Ki of 0.25-1.2 nM and also inhibits 5-HT receptor (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) with Ki of 0.03-4.0 nM. |
| M5400 | Alosetron | Alosetron Hydrochloride is the hydrochloride salt form of alosetron, a potent and selective 5-HT3 receptor antagonist. |
| M5214 | Lasmiditan hydrochloride | Lasmiditan hydrochloride (also known as COL-144 and LY573144) is a high-affinity, highly selective serotonin (5-HT) 5-HT(1F) receptor agonist. |
| M5130 | Cisapride | Cisapride(R 51619) is a nonselective 5-HT4 receptor agonist, it is also a potent hERG potassium channel inhibitor. IC50 Value is 0.14 μM (EC50 for 5-HT4 receptor). |
| M5045 | Tianeptine | Tianeptine is a selective facilitator of 5-HT uptake in vitro and in vivo. |
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