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Cat. No. Product Name Information
PC-21668

PZ-1444

5-HT6R inverse agonist

PZ-1444 is a potent, selective partial inverse agonist of 5-HT6 receptor with Ki of 6 nM, IC50 (Gs) of 17.6 nM.
PC-21667

PZ-1922

5-HT6 antagonist

PZ-1922 is a potent, triple-acting 5-HT6R/5-HT3R antagonist and MAO-B reversible inhibitor with Ki of 17/0.45 nM (5-HT6R/5-HT3R), and pIC50 of 8.93 for MAO-B.
PC-21666

5-HT6 receptor antagonist 15

5-HT6 antagonist

5-HT6 receptor antagonist 15 is a first-in-class, selenium containing, highly potent and selective 5-HT6R antagonist with Ki of 14 nM.
PC-21178

25B-NBOMe

5-HT2A agonist

25B-NBOMe is a highly selective 5-HT2A receptor agonist with Ki of 0.05 nM, 100-fold selective over 5-HT2C (Ki=4.6 nM).
PC-21048

NU-1223

5-HT2C agonist

NU-1223 is a β carboline analog of alstonine and serotonin 5-HT2C receptor agonist, blocks phencyclidine and amphetamine-induced hyperactivity in subchronic phencyclidine mice.
PC-20963

Pimavanserin

5-HT2A inverse agonist

Pimavanserin (ACP-103) is a potent, selective, orally active 5-HT2A receptor inverse agonist, competitively antagonizes the binding of [(3)H]ketanserin to heterologously expressed human 5-HT(2A) receptors with pKi of 9.3 in membranes and 9.70 in whole cells.
PC-20845

EMD386088 hydrochloride

5-HT6 agonist

EMD386088 hydrochloride is a potent, selective 5-HT6 receptor agonist with EC50 of 1.0 nM.
PC-20844

EMD386088

5-HT6 agonist

EMD386088 is a potent, selective 5-HT6 receptor agonist with EC50 of 1.0 nM.
PC-20843

SAM-531

5-HT6 agonist

SAM-531 (Cerlapirdine, WAY-262531) is a selective, highly potent, 5-HT6 receptor antagonist.
PC-49806

5-HT2A agonist (R)-70

5-HT2A agonist (R)-70 is a potent selective 5-HT2A receptor partial agonist with EC50 of 110 nM in calcium flux assays, and Ki value of 880 nM.
PC-49805

5-HT2A agonist (R)-69

5-HT2A agonist (R)-69 is a potent selective 5-HT2A receptor partial agonist with EC50 of 41 nM in calcium flux assays, and Ki value of 680 nM.
PC-49160

ASP5736

5-HT5A antagonist

AS5736 is a potent, selective and brain-penetrating 5-HT5A receptor antagonist with Ki of 3.6, 1.7 and 4.4 nM against human, rat, mouse 5-HT5A receptors, respectively.

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