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). |