GLPBio

Dopamine Transporter

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Dopamine Transporter (DAT) is an integral membrane protein that removes dopamine from the synaptic cleft and deposits it into surrounding cells, thus terminating the signal of the neurotransmitter. Dopamine transporter (DAT) controls the spatial and temporal dynamics of dopamine (DA) neurotransmission by driving reuptake of extracellular transmitter into presynaptic neurons. Many diseases such as depression, bipolar disorder, Parkinson’s disease, and attention deficit hyperactivity disorder are associated with abnormal DA levels, implicating DAT as a factor in their etiology. Medications used to treat these disorders and many addictive drugs target DAT and enhance dopaminergic signaling by suppressing transmitter reuptake. DAT is regulated by multiple signaling systems, with PKC and ERK being two of the most well-characterized.

Products Related to Dopamine Transporter(20)

  • GC10126 structure
    GC10126Desipramine hydrochloride
    CAS: 58-28-6
    Purity: >99.00%

    Desipramine hydrochloride is a tricyclic antidepressant.

  • 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

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

    potent and selective DRI (Dopamine reuptake inhibitor)

  • GC19117 structure
    GC19117Dasotraline
    CAS: 675126-05-3
    Purity: >98%

    Dasotraline is a triple reuptake inhibitor that blocks dopamine, norepinephrine, and serotonin transporters with IC50 values of 4, 6, and 11 nM, respectively.

  • GC19118 structure
    GC19118Dasotraline hydrochloride
    CAS: 675126-08-6
    Purity: >99.50%

    Dasotraline hydrochloride (SEP-225289 hydrochloride) is a triple reuptake inhibitor that blocks dopamine, norepinephrine, and serotonin transporters with IC50 values of 4, 6, and 11 nM, respectively.

  • GC30780 structure
    GC30780Fipexide
    CAS: 34161-24-5
    Purity: >98.00%

    Fipexide, a parachloro-phenossiacetic acid derivative, is a nootropic drug.

  • GC30981 structure
    GC30981Amitifadine hydrochloride (DOV-21947 hydrochloride)
    CAS: 410074-74-7
    Purity: >99.50%

    Amitifadine hydrochloride (DOV-21947 hydrochloride) is a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI), with IC50s of 12, 23, 96 nM for serotonin, norepinephrine and dopamine in HEK 293 cells , respectively.

  • GC31020 structure
    GC31020SPD-473 citrate
    CAS: 161190-26-7
    Purity: >98%

    SPD-473 citrate is a serotonin/dopamine/norepinephrine reuptake inhibitior.

  • GC31175 structure
    GC31175Centanafadine hydrochloride (EB-1020 (hydrochloride))
    CAS: 923981-14-0
    Purity: >99.50%

    Centanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter, with IC50s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.

  • GC31283 structure
    GC31283Centanafadine (EB-1020)
    CAS: 924012-43-1
    Purity: >98%

    Centanafadine (EB-1020) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter, with IC50s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.

  • GC33711 structure
    GC33711Diclofensine (Ro 8-4650)
    CAS: 67165-56-4
    Purity: >98%

    Diclofensine (Ro 8-4650)(Ro-8-4650) is a potent inhibitor of monoamine reuptake, blocking the uptake of dopamine, noradrenaline, and serotonin by rat brain synaptosomes with IC50 values of 0.74, 2.3, and 3.7 nM, respectively.

  • GC33713 structure
    GC33713Levophacetoperane hydrochloride
    CAS: 23257-56-9
    Purity: >98%
  • GC34559 structure
    GC34559DOV-216,303 Free Base
    CAS: 66504-40-3
    Purity: >98.00%

    DOV-216,303 (Free Base) is a potent triple serotonin, norepinephrine, and dopamine reuptake inhibitor, with IC50 values of 14 nM, 20 nM and 78 nM for hSERT, hNET and hDAT, respectively.

  • GC36126 structure
    GC36126GBR 12935
    CAS: 76778-22-8
    Purity: >98%

    GBR 12935 is a potent, and selective dopamine reuptake inhibitor.

  • GC60527 structure
    GC605275,7-Dimethoxyluteolin
    CAS: 90363-40-9
    Purity: >98%

    5,7-Dimethoxyluteolin, a 5,7-dimethylluteolin derivative, is a dopamine transporter (DAT) activator with an EC50 of 3.417 μM.

  • GC70490 structure
    GC70490BMS-466442
    CAS: 1598424-76-0
    Purity: >98.00%

    BMS-466442 is a potent and selective inhibitor of asc-1 (alanine serine cysteine transporter-1), with an IC50 of 11 nM.

  • GC71317 structure
    GC71317Z1078601926
    CAS: 1493256-85-1
    Purity: >98.00%

    Z1078601926 is an allosterical inhibitor of human dopamine transporter (hDAT).

  • GC73772 structure
    GC73772JJC8-088 dioxalate
    CAS: 2068692-71-5
    Purity: >99.00%

    JJC8-088 dioxalate is the dioxalate salt form of JJC8-088.

  • GC81886 structure
    GC81886(S)-Phenylpiracetam
    CAS: 949925-08-0
    Purity: >98.00%

    (S)-Phenylpiracetam ((S)-Carphedon; (S)-Fonturacetam; (S)-MRZ 9547) is an orally active and selective dopamine transporter inhibitor, with K i = 56 μM.