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Request The Product List ofTrace Amine-associated Receptor (TAAR) Trace Amine-associated Receptor (TAAR)

Cat. No. Product Name Information
PC-72628

Ralmitaront

TAAR1 modulator

Ralmitaront (RO6889450, RG7906) is a potent, orally active trace amine-associated receptor 1 (TAAR-1) modulator as a neuroleptic agent.
PC-72627

Ulotaront

TAAR1 agonist

Ulotaront (SEP-363856, SEP-856) is a novel psychotropic agent with agonism at trace amine receptor 1 (TAAR1) and 5-HT1A receptors but no appreciable action at dopamine D2 receptors.
PC-61078

Alpha-NETA free base

Alpha-NETA is a selective choline acetyltransferase (ChA) inhibitor with IC50 of 9 uM, also is a TAAR5 agonist that affects sensory gating in rats.
PC-61077

RO 5203648

RO 5203648 is a potent and selective TAAR1 partial agonist with Ki of 0.5, 1.0, 6.8 and 2.6 nM for mouse, rat, human and monkey TAAR1, respectively.
PC-61075

RO 5166017

TAAR1 agonist

RO 5166017 is a potent, selective TAAR1 agonist with Ki of 1.9, 2.7, 31 and 24 nM for mouse, rat, cynomolgus monkey and human TAAR1 stably expressed in HEK293 cells.
PC-61073

EPPTB

EPPTB (RO5212773) is a potent, selective mouse TAAR1 antagonist that potently antagonizes cAMP production induced by 1.5 uM β-phenylethylamine with IC50 of 27.5 nM, Ki of 1 nM.
PC-61072

RO 5263397

TAAR1 agonist

RO 5263397 is a highly potent, selective and orally bioavailable trace amine-associated receptor 1 (TAAR1) partial agonist with EC50 of 17 nM, >1,000-fold selectivity over human adrenergic α2A receptor.
PC-72353

RTI-7470-44

hTAAR1 antagonist

RTI-7470-44 is a potent, selective human trace amine-associated receptor subtype 1 (hTAAR1) inhibitor with IC50 of 8.4 nM in vitro cAMP functional assay.
PC-61076

RO 5073012

A potent, selective, orally active TAAR1 partial agonist with Ki of 6 nM, EC50 of 23 nM (hTAAR1), 140-fold selectivity over β2 adrenergic receptors.
PC-61074

Ractopamine

A small molecule TAAR1 agonist and β adrenoreceptor agonist that stimulates β1 and β2 adrenergic receptors.
PC-61071

RO 5256390

A highly potent, selective and orally bioavailable trace amine-associated receptor 1 (TRRA1) full agonist with EC50 of 18 nM, >500-fold selectivity over human adrenergic α2A receptor.

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