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Dopamine Receptor

Dopamine Receptor

In the central nervous system (CNS) of vertebrates, dopamine receptors are a class of G protein-coupled receptors that are widely distributed. The main endogenous ligand for dopamine receptors is the neurotransmitter dopamine. Numerous neurological functions, including motivation, pleasure, cognition, memory, learning, and fine motor control, as well as the modulation of neuroendocrine signaling, are associated with dopamine receptors.Numerous neuropsychiatric disorders have abnormal dopamine receptor signaling and dopaminergic nerve function at their core. Dopamine receptors are therefore typical neurologic drug targets; psychostimulants are typically indirect agonists of dopamine receptors, whereas antipsychotics are frequently dopamine receptor antagonists. Dopamine receptors come in at least five different subtypes: D1, D2, D3, D4, and D5. The D2, D3, and D4 dopamine receptors are members of the D2-like family, whereas the D1 and D5 receptors belong to the D1-like family.

Dopamine Receptor related products

Structure Cat No. Product Name CAS No. Product Description
GBR 12783 dihydrochloride V71729 GBR 12783 dihydrochloride 67469-75-4 GBR 12783 di-HCl is a specific, potent and specific dopamine uptake inhibitor that can suppress the uptake of [3H]dopamine ([3H]dopamine) by striatal synaptosomes in rats and mice, with IC50 of 1.8 nM and 1.2 nM.
GBR-12879 dihydrochloride V71767 GBR-12879 dihydrochloride 67469-45-8 GBR-12879 diHCl is a potent dopamine uptake inhibitor.
Glovadalenum V99968 Glovadalenum 2576359-31-2 Glovadalenum (Glovadalen) is a dopamine D1 receptor positive allosteric modulator.
GR 103691 V2454 GR 103691 162408-66-4 GR 103691 is a potent and specific dopamine D3 receptor blocker (antagonist) with Ki of 0.4 nM.
GSK598809 V71717 GSK598809 863680-45-9 GSK598809 is a selective antagonist of dopamine D3 receptor (DRD3) with pKi of 8.9.
Haloperidol-d4 N-Oxide (haloperidol d4 (N-oxide)) V71742 Haloperidol-d4 N-Oxide (haloperidol d4 (N-oxide)) 1246815-56-4 Haloperidol-d4 N-Oxide is the deuterium labelled form of Haloperidol.
ITI-722 (Lumateperone) V22774 ITI-722 (Lumateperone) 313368-91-1 Lumateperone (ITI-722; ITI722; Caplyta) is a novel, potent, first-in-class and dual 5HT2A receptor antagonist and dopamine receptor phosphoprotein modulator (DPPM).
JHW007 hydrochloride V71776 JHW007 hydrochloride 202645-74-7 JHW007 HCl is the HCl of JHW007.
KEMPFPKYPVEP V101770 KEMPFPKYPVEP 1393589-51-9 KEMPFPKYPVEP is a neuropeptide composed of 12 amino acids.
LB-102 V94042 LB-102 2227154-23-4 LB-102 is an oral dopamine D2, D3, and 5-HT7 receptor inhibitor that can be used in the research of schizophrenia and other psychiatric disorders.
LE 300 V71153 LE 300 274694-98-3 LE 300 is a potent and specific dopamine D1-like receptor antagonist (inhibitor) with Kis of 1.9 nM and 7.5 nM in CHO cell membranes expressing human dopamine D1 and D5 receptors, respectively.
Matsupexolum V99973 Matsupexolum 1399442-97-7 Matsupexolum (Matsupexole) is a dopamine receptor agonist.
Mesdopetam (IRL790) V71737 Mesdopetam (IRL790) 1403894-72-3 Mesdopetam (IRL790) is a dopamine D3 receptor antagonist (Ki=90 nM; IC50=9.8 μM) with psychomotor stabilizing properties.
Mesdopetam hemitartrate (IRL790 hemitartrate) V71725 Mesdopetam hemitartrate (IRL790 hemitartrate) 2562346-14-7 Mesdopetam (IRL790) hemitartrate is a dopamine D3 receptor antagonist (Ki=90 nM; IC50=9.8 μM) with psychomotor stabilizing properties.
MeSeI V89037 MeSeI 2901664-87-5 MeSeI exhibits weak inhibitory activity against monoamine oxidase MAO-A and MAO-B (IC50=198.8 µM).
Mesulergine hydrochloride (CU32-085 hydrochloride) V84639 Mesulergine hydrochloride (CU32-085 hydrochloride) 72786-12-0 Mesulergine (CU32-085) hydrochloride is a potent 5-HT2C antagonist and dopamine (DA) agonist.
MIF-1 TFA (Pro-Leu-Gly-NH2 TFA; Melanostatin TFA) V71731 MIF-1 TFA (Pro-Leu-Gly-NH2 TFA; Melanostatin TFA) 35240-69-8 MIF-1 TFA (Melanostatin) is an endogenous brain peptide and a potent allosteric modulator of dopamine receptors.
ML417 V37653 ML417 1386162-69-1 ML417 is a novel and selective agonist of D3 dopamine receptor, it potently promotes D3R-mediated β-arrestin translocation, G protein activation, and ERK1/2 phosphorylation (pERK) while lacking activity at other dopamine receptors.
Moperone V107743 Moperone 1050-79-9 Moperone (R 1658) is a D2 dopamine receptor and D3 dopamine receptor antagonist with IC50 of 1.0 nM and 1.0 nM, respectively.
MPTP hydrochloride V2705 MPTP hydrochloride 23007-85-4 MPTP hydrochloride is a dopaminergic neurotoxin and cause selective destruction of dopaminergic neurons in animal models of parkinsonism.
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