GLPBio

Dopamine Receptor

Dopamine receptors (DR) are members of G protein-coupled receptors superfamily. There are 5 subtypes (D1, D2, D3, D4, D5) of DR which mediate the functions of dopamine in central nervous system for control of locomotion, cognition, and emotion etc.

Products Related to Dopamine Receptor(300)

  • GC10105 structure
    GC10105Amantadine HCl
    CAS: 665-66-7
    Purity: >98.00%

    Amantadine (1-Adamantanamine) hydrochloride is an orally avtive and potent antiviral agent with activity against influenza A viruses.

  • GC10112 structure
    GC10112Paliperidone
    CAS: 144598-75-4
    Purity: >99.50%

    Dopamine receptor antagonist

  • GC10117 structure
    GC10117Aripiprazole
    CAS: 129722-12-9
    Purity: >99.50%

    5-HT receptor partial agonist

  • GC10144 structure
    GC10144Domperidone
    CAS: 57808-66-9
    Purity: >99.50%

    Drug for gastroparesis

  • GC11028 structure
    GC11028Dopamine HCl
    CAS: 62-31-7
    Purity: >98.50%

    Dopamine D1-5 receptors agonist

  • GC11182 structure
    GC11182LY404039
    CAS: 635318-11-5
    Purity: >98.00%

    MGlu2 and mGlu3 receptors agonist

  • GC11186 structure
    GC11186Brexpiprazole
    CAS: 913611-97-9
    Purity: >97.00%

    Brexpiprazole, an oral atypical antipsychotic agent, is a potent partial agonist of 5-HT1A (K i =0.12nM) and dopamine D2L (K i =0.3nM) receptors, and an antagonist of 5-HT2A receptor (K i =0.47nM).

  • GC11506 structure
    GC11506Haloperidol hydrochloride
    CAS: 1511-16-6
    Purity: >98%

    Antipsychotic drug

  • GC11960 structure
    GC11960Pramipexole
    CAS: 104632-26-0
    Purity: >99.50%

    Dopamine agonist

  • GC12610 structure
    GC12610Amisulpride
    CAS: 71675-85-9
    Purity: >99.50%

    Dopamine D2/D3 receptor antagonist

  • GC13322 structure
    GC13322Vanoxerine
    CAS: 67469-69-6
    Purity: >98%

    potent and selective DRI (Dopamine reuptake inhibitor)

  • GC13853 structure
    GC13853GBR 12935 dihydrochloride
    CAS: 67469-81-2
    Purity: >98.00%

    dopamine reuptake inhibitor

  • GC14216 structure
    GC14216Chlorpromazine HCl
    CAS: 69-09-0
    Purity: >99.50%

    Chlorpromazine HCl is an orally effective, blood-brain-permeable phenothiazine antipsychotic that can effectively antagonize D2 dopamine receptors and 5-HT 2A and has a strong sedative effect.

  • GC14759 structure
    GC14759Fenoldopam
    CAS: 67227-56-9
    Purity: >98%

    D1-like dopamine receptor partial agonist

  • GC15095 structure
    GC15095Levodopa
    CAS: 59-92-7
    Purity: >99.00%

    Levodopa (Levodopa) is an orally active metabolic precursor of neurotransmitters dopamine.

  • GC15312 structure
    GC15312Chlorprothixene
    CAS: 113-59-7
    Purity: >99.00%

    Dopamine receptor antagonist

  • GC15470 structure
    GC15470Levosulpiride
    CAS: 23672-07-3
    Purity: >99.50%

    Antipsychotic drug

  • GC16615 structure
    GC16615Pergolide mesylate
    CAS: 66104-23-2
    Purity: >99.50%

    Dopaminergic agonist

  • GC16783 structure
    GC16783Pramipexole 2HCl Monohydrate
    CAS: 191217-81-9
    Purity: >98.00%

    Pramipexole 2HCl Monohydrate is a selective and blood-brain barrier (BBB) penetrant dopamine D2-type receptor agonist, with Kis of 2.2 nM, 3.9 nM, 0.5 nM and 1.3 nM for D2-type receptor, D2, D3 and D4 receptors, respectively.

  • GC16891 structure
    GC16891Quetiapine Fumarate
    CAS: 111974-72-2
    Purity: >98.00%

    Quetiapine Fumarate is a 5-HT receptors agonist with a pEC50 of 4.77 for human 5-HT1A receptor.

  • GC17184 structure
    GC17184Ambrisentan
    CAS: 177036-94-1
    Purity: >99.50%

    Ambrisentan is an orally active, highly selective antagonist of endothelin receptor ETA-selective antagonist, with an IC 50 value of 0.6nM.

  • GC17599 structure
    GC17599Haloperidol
    CAS: 52-86-8
    Purity: >98.00%

    Haloperidol is a classic antipsychotic and dopamine D2-like receptor antagonist, as well as an ion channel inhibitor that inhibits a variety of ion channels, such as G-protein-activated inwardly rectifying potassium channels, calcium-activated potassium channels, HERG and HEAG potassium channels, as well as L-, N- and P-type calcium channels.

  • GC17600 structure
    GC17600PD128907 HCl
    CAS: 112960-16-4
    Purity: >98%

    Potent and selective dopamine D3 receptor agonist

  • GC17741 structure
    GC17741Vanoxerine dihydrochloride
    CAS: 67469-78-7
    Purity: >98.00%

    potent and selective DRI (Dopamine reuptake inhibitor)