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Cat. No. Product Name Information
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.
PC-61583

GSK-588045

5-HT1A/B/D antagonist

GSK-588045 is a potent and selective 5-HT1A/B/D receptor antagonist with Ki of 9.5/8.8/9.8, respectively.
PC-61522

SUVN-502 mesylate hydrate

5-HT6 antagonist

SUVN-502 mesylate hydrate (SUVN502) is a potent, selective, brain penetrant and orally active 5-HT6 receptor antagonist with Ki of 2.04 nM.
PC-61521

SUVN-502 mesylate

5-HT6 antagonist

SUVN-502 (Masupirdine, SUVN502) mesylate is a potent, selective, brain penetrant and orally active 5-HT6 receptor antagonist with Ki of 2.04 nM.
PC-61511

AVN-211

5-HT6 antagonist

AVN-211 (CD-008-0173) is a novel and highly selective 5-HT6 receptor small molecule antagonist with Ki of 2.34 nM.
PC-61504

AVN-101

5-HT7 antagonist

AVN-101 is a higly potent, orally bioavailable, BBB permeable 5-HT7 receptor antagonist with Ki of 153 pM, with slightly lesser potency toward 5-HT6, 5-HT2A and 5HT-2C (Ki = 1.2-2.0  nM).

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