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Cat. No. Product Name Information
PC-62093

YH12852

5-HT4 agonist

YH12852 is a potent, highly selective 5-HT4 receptor agonist with pKi of 10.3, exhibits more potent agonistic activity (pEC50=11.4) than both tegaserod and prucalopride.
PC-62010

VA-012

5-HT2C PAM

VA-012 is a potent, selective 5-HT2C receptor positive allosteric modulator (PAM) that exhibits dose-dependent potentiation of 5-HT efficacy with EC50 of 16 nM.
PC-61883

PF-03382792

5-HT4 agonist

PF-03382792 is a potent, brain penetrant 5-HT4 partial agonist with Ki of 2.7 nM and an EC50 of 0.9 nM for 5-HT4d, produces moderate increases in cortical Ach in the rat prefrontal cortex.
PC-61868

Eletriptan

5-HT1B/1D agonist

Eletriptan (UK 116044) is a potent, selective, and orally active 5-HT1B/1D receptor agonist with pKi of 8.0 and 8.9.
PC-61867

Eletriptan hydrobromide

5-HT1B/1D agonist

Eletriptan (UK 116044) hydrobromide is a potent, selective, and orally active 5-HT1B/1D receptor agonist with Ki of 0.92 nM and 3.14 nM respectively.
PC-61866

GR127935 hydrochloride

5-HT1B/1D antagonist

GR-127935 potent and selective 5-HT1B/1D receptor antagonist with pKi of 8.5 for both guinea pig 5-HT1D and rat 5-HT1B receptor.
PC-61865

GR127935

5-HT1B/1D antagonist

GR127935 is a potent and selective 5-HT1B/1D receptor antagonist with pKi of 8.5 for both guinea pig 5-HT1D and rat 5-HT1B receptor.
PC-61831

PF-04995274

5-HT4 agonist

PF-04995274 (PF-4995274, TBPT) is a potent, selective, orally active and partial serotonin 4 receptor (5-HT4R) agonist with Ki of 0.15-0.46 nM.
PC-61814

SB737050A

5-HT6 antagonist

SB 737050A is a potent, selective 5-HT6 receptor antagonist to prevent relapse intio addiction.
PC-61812

GSK-812

GSK-812 is a potent neuroprotectant that can induce GDNF in normal and diseased retina, shows has polypharmacology antagonizing multiple receptors, including D2 and D3 receptors, and 5-HT2A, 2C, and 5-HT6 receptors.
PC-61729

Revexepride

5-HT4 agonist

Revexepride (SSP 002358, SPD-557) is a potent, highly selective 5-HT4 receptor agonist for the treatment of gastroesophageal reflux disease.
PC-61625

Befiradol

5-HT1A agonist

Befiradol (F13640, NLX 112) is a highly potent, selective 5-HT1A receptor agonist with Ki of 2.7 nM.

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