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Nitrocaramiphen hydrochloride is an antagonist of muscarinic acetylcholine receptor M1 (mAChR M1) which can completely remove the hyperpolarizing effect of muscarine
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Duloxetine (LY-248686) is a potent inhibitor of serotonin (5-hydroxytryptamine 5-HT) and noradrenaline (NE) uptake in vitro and in vivo and is 3- to 5-times more effective at inhibiting 5-HT uptake
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Duloxetine HCl (LY-248686) is a serotonin-norepinephrine reuptake inhibitor with Ki of 4 6 nM used for treatment of major depressive disorder and generalized anxiety disorder (GAD)
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VU 0364770 is a positive allosteric modulator(PAM) of mGlu4 with EC50 of 1 1 M exhibits insignificant activity at 68 other receptors including other mGlu subtypes
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N-Acetyl-5-hydroxytryptamine (NAS N-Acetylserotonin Normelatonin O-Demethylmelatonin) a precursor of melatonin is a potent and selective agonist of TrkB receptor
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RS-127445 (MT500) is a selective 5-HT2B receptor antagonist with pKi of 9 5 and pIC50 of 10 4 exhibits 1000-fold selectivity against other 5-HT receptors
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VU-29 is a positive allosteric modulator of metabotropic glutamate 5 (mGlu5) receptor with EC50 of 9 nM and Ki 244 nM for rat mGluR5 which is selective for mGluR5 relative to other mGluR subtypes
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VU 0361737 is a selective positive allosteric modulator (PAM) for mGlu4 receptor with EC50 of 240 nM and 110 nM at human and rat receptors respectively displays weak activity at mGlu5 and mGlu8 receptors is inactive at mGlu1 mGlu2 mGlu3 mGlu6 and mGlu7 receptors can penetrate into CNS
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VU0357121 is a novel positive allosteric modulator (PAM) of mGlu5 with EC50 of 33 nM is inactive or very weakly antagonizing at other mGlu receptor subtypes
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