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Trace amine-associated receptors are a class of G-protein-coupled receptors, identified in human (six subtypes) and other vertebrates and invertebrates.

TAAR

货号 产品名 CAS号 信息
CSN25153 2-(1H-Indol-3-yl)ethanamine 61-54-1 Tryptamine is a monoamine alkaloid and may play a role as a neuromodulator or neurotransmitter. It is an agonist of hTAAR1. It acts as a non-selective serotonin receptor agonist and serotonin-norepinephrine-dopamine releasing agent (SNDRA).
CSN26560 SEP-363856 1310426-33-5 SEP-363856 (SEP-856), an orally active and CNS active psychotropic agent with a unique, non-D2/5-HT2A mechanism of action, exerts its antipsychotic-like effects. SEP-363856 (SEP-856) has the potential for the treatment of schizophrenia[1].
CSN26364 RO5263397 1357266-05-7 RO5263397 is a potent, selective, and orally available TAAR1 agonist, with EC50s of 17 and 35 nM for human TAAR1 and rat TAAR1, respectively. RO5263397 regulates wakefulness and EEG spectral composition and shows antidepressant-like effect[1][2][3].
CSN26256 RO5256390 1043495-96-0 RO5256390 is an agonist of trace amine-associated receptor 1 (TAAR1), a highly conserved G-protein-coupled receptor (GPCR) bound by endogenous trace amines. RO5256390 blocks psychostimulant-induced hyperactivity and produces a brain activation pattern reminiscent of the antipsychotic drug olanzapine, suggesting antipsychotic-like properties.
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