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Cat. No. Product Name Information
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-38596

SB 224289 hydrochloride

5-HT1B antagonist

SB 224289 hydrochloride is a potent, selective 5-HT1B inverse agonist/antagonist with pKi value of 8.16, displays >75-fold selectivity over all other 5-HT receptors.
PC-73302

AVN-492

5-HT6 antagonist

AVN-492 is a highly potent and selective 5-HT6 receptor antagonist with Ki of 91 pM, >1000-fold selectivity over 5-HT2BR (Ki=170 nM).
PC-73301

ST1936 oxalate

5-HT6 agonist

ST1936 is a potent, selective 5-HT6 receptor agonist with Ki of 13 nM, >10-fold selectivity over 5-HT7 and 5-HT2B receptors.
PC-73300

LP-211

5-HT7 agonist

LP-211 is a potent, selective, and BBB-penetrant 5-HT7 receptor agonist with Ki of 0.58 nM, high selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM).
PC-73299

Usmarapride

5-HT4 agonist

Usmarapride (SUVN-D4010) is a potent, selective, orally active and brain penetrant 5-HT4 receptor partial agonist with EC50of 44 nM.
PC-45693

Lumateperone tosylate

Lumateperone (ITI-007) is a potent 5-HT2A antagonist (Ki=0.54 nM), postsynaptic D2 antagonist(Ki=32 nM), and SERT blocker (Ki= 61 nM).
PC-45233

Iloperidone hydrochloride

An atypical antipsychotic that exhibits high affinity to serotonin 5HT2A (Ki =5.6 nM), dopamine D2 (Ki=6.3 nM) and D3 (Ki=7.1 nM) and noradrenaline α1 receptors (Ki=0.36 nM), moderate affinity for D4 (25 nM), 5HT6 (43 nM), 5HT7 (22 nM), and low affinity for 5HT1A (168 nM), D1 and histamine H1 receptors.
PC-42792

Risperidone mesylate

An antipsychotic agent with serotonin-S2 and dopamine-D2 antagonistic properties.
PC-42791

Risperidone hydrochloride

An antipsychotic agent with serotonin-S2 and dopamine-D2 antagonistic properties.

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