Catalog |
name |
Description |
price |
R-R-4288 |
Oxidopamine hydrochloride CAS No.28094-15-7 |
Oxidopamine (6-OHDA) hydrochloride/CAS No.28094-15-7 is an antagonist of the neurotransmitter dopamine. Oxidopamine hydrochloride is a widely used neurotoxin and selectively destroys dopaminergic neurons. Oxidopamine hydrochloride promotes COX-2 activation, leading to PGE2 synthesis and pro-inflammatory cytokine IL-1β secretion. |
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R-R-4289 |
SKF 81297 CAS No.71636-61-8 |
SKF 81297/CAS No.71636-61-8 is a potent and selective dopamine D1 receptor agonist. |
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R-R-4290 |
Fallypride CAS No.166173-78-0 |
Fallypride/CAS No.166173-78-0 is a potent antagonist of dopamine D2/D3 receptor. Fallypride, in the form of fallypride (18F), can be used as a positron emission tomography (PET) radiotracer. |
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R-C-2591 |
GRI 977143 CAS:325850-81-5 |
GRI977143 is a selective lysophosphatidic acid 2(LPA2)receptor non-lipid agonist (EC50=3.3μM).GRI977143 does not activate other LPA GPCRs at concentrations up to 10μM. |
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R-R-4291 |
Octoclothepin maleate salt CAS No.4789-68-8 |
Octoclothepin maleate salt/CAS No.4789-68-8, an orally active neuroleptic agent, is a dual SR-2A and D2DR inhibitor. Octoclothepin maleate salt reveals an intensive central depressant action in a series of observational and instrumental procedures in rodents. |
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R-R-4292 |
Clozapine N-oxide dihydrochloride CAS No.2250025-93-3 |
Clozapine N-oxide dihydrochloride/CAS No.2250025-93-3 is a major metabolite of Clozapine and a human muscarinic designer receptors (DREADDs) agonist. Clozapine N-oxide dihydrochloride activates the DREADD receptor hM3Dq and hM4Di. Clozapine N-oxide dihydrochloride can cross the blood-brain barrier. Clozapine is a potent dopamine antagonist and also a potent and selective muscarinic M4 receptor (EC50=11 nM) agonist. |
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R-R-4293 |
SKF 38393 hydrochloride CAS No.62717-42-4 |
SKF 38393 hydrochloride/CAS No.62717-42-4 is a selective agonist of the dopamine D1 receptor (D1DR) with an IC50 of 110 nM. |
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R-R-4294 |
Cabergoline CAS No.81409-90-7 |
Cabergoline/CAS No.81409-90-7 is an ergot derived-dopamine D2-like receptor agonist that has high affinity for D2, D3, and 5-HT2B receptors (Ki=0.7, 1.5, and 1.2, respectively). |
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R-R-4295 |
Fluphenazine dihydrochloride CAS No.146-56-5 |
Fluphenazine dihydrochloride/CAS No.146-56-5 is a potent, orally active phenothiazine-based dopamine receptor antagonist. Fluphenazine dihydrochloride blocks neuronal voltage-gated sodium channels. Fluphenazine dihydrochloride acts primarily through antagonism of postsynaptic dopamine-2 receptors in mesolimbic, nigrostriatal, and tuberoinfundibular neural pathways. Fluphenazine dihydrochloride can antagonize Methylphenidate-induced stereotyped gnawing and inhibit climbing behaviour in mice. Fluphenazine dihydrochloride can be used for researching psychosis and painful peripheral neuropathy associated with diabetes and has potential to inhibit SARS-CoV-2. |
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R-R-4296 |
ONC206 CAS No.1638178-87-6 |
ONC206/CAS No.1638178-87-6 is an analogue of TRAIL inducer ONC201. ONC206 is a selective antagonist of the D2-like dopamine receptors (DRD2/3/4) at nanomolar concentrations. ONC206 has broad-spectrum anti-tumor activity. |
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