1. Signaling Pathways
  2. Neuronal Signaling
  3. Dopamine Transporter

Dopamine Transporter

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.

Dopamine Transporter 相关产品 (17):

Cat. No. Product Name Effect Purity
  • HY-13217
    Vanoxerine dihydrochloride Inhibitor 99.52%
    Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) 是竞争性的,有效选择性的多巴胺再摄取 (dopamine reuptake) 抑制剂。Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) 与多巴胺转运体 (DAT) 上的靶点结合。
  • HY-B1272
    Desipramine hydrochloride Inhibitor 99.68%
    Desipramine hydrochloride 是去甲肾上腺素转运蛋白 (NET), 5-羟色胺转运体 (SERT) 和多巴胺转运 (DAT) 的抑制剂,其 Ki 值分别为 4, 61 和 78,720 nM。
  • HY-B1124
    Fipexide Inhibitor 99.88%
    Fipexide是一种哌嗪类的抗精神药物, 用作一种健脑药, 主要用于治疗老年痴呆。
  • HY-13779
    J-147 Inhibitor 99.90%
    J-147 是一种特别有效的,具有口服活性的神经保护剂,可增强认知能力。J-147 可透过血脑屏障 (BBB)。J-147 抑制单胺氧化酶 B (MAO B) 和多巴胺转运体 (dopamine transporter),EC50 分别为 1.88 μM 和 0.649 μM。J-147 有潜力用于阿尔茨海默氏症 (AD) 的研究。
  • HY-18332A
    Amitifadine hydrochloride Inhibitor 99.92%
    Amitifadine hydrochloride 是5-羟色胺-去甲肾上腺素-多巴胺的再摄取抑制剂 (SNDRI),其在 HEK 293 细胞中测得的 IC50 值分别为 12, 23, 96 nM。
  • HY-12850A
    Dasotraline hydrochloride Inhibitor 99.55%
    Dasotraline hydrochloride (SEP-225289 hydrochloride) 是具有阻断多巴胺,去甲肾上腺素和三羟色胺转运蛋白的三重再摄取抑制剂,IC50值分别为4,6和11 nM。
  • HY-16736A
    Centanafadine hydrochloride Inhibitor 99.93%
    Centanafadine (hydrochloride) 是去甲肾上腺素 (NE)/多巴胺 (DA) 转运的双抑制剂,还能抑制5-羟色胺 (serotonin) 转运体,其对人 NE,DA 和5-羟色胺转运体的IC50 值分别为6 nM,38 nM 和 83 nM。
  • HY-12242
    GBR 12935 dihydrochloride Inhibitor 98.90%
    GBR 12935 dihydrochloride 是多巴胺再吸收抑制剂。
  • HY-12850
    Dasotraline Inhibitor
    Dasotraline 是一种三重再摄取抑制剂,阻断多巴胺 (dopamine),去甲肾上腺素 (norepinephrine) 和 5-羟色胺 (5-HT) 转运蛋白,IC50 值分别为 4, 6 和 11 nM。
  • HY-18332C
    DOV-216,303 Free Base Inhibitor 98.47%
    DOV-216,303 (Free Base) 是有效的 5-羟色胺、去甲肾上腺素、多巴胺再摄取的三重抑制剂,其对 hSERT、hNET 和 hDAT 的 IC50 值分别为 14 nM,20 nM和78 nM。在嗅球切除大鼠模型中,可增加前额皮质中单胺的释放及具有抗抑郁的作用。
  • HY-18610
    Diclofensine hydrochloride Inhibitor
    Diclofensine hydrochloride (Ro-8-4650 hydrochloride) 是高效单胺再摄取抑制剂,大鼠脑突触体中阻断多巴胺、去甲肾上腺素和5-羟色胺的IC50值分别为0.74、2.3和3.7nM。
  • HY-13217A
    Vanoxerine Inhibitor
    Vanoxerine (GBR-12909) 是竞争性的,有效选择性的多巴胺再摄取 (dopamine reuptake) 抑制剂。Vanoxerine (GBR-12909) 与多巴胺转运体 (DAT) 上的靶点结合。
  • HY-12242A
    GBR 12935 Inhibitor
    GBR 12935是多巴胺再吸收抑制剂。
  • HY-18610A
    Diclofensine Inhibitor
    Diclofensine(Ro-8-4650)是高效单胺再摄取抑制剂,大鼠脑突触体中阻断多巴胺、去甲肾上腺素和5-羟色胺的IC50值分别为0.74、2.3和3.7nM。
  • HY-101631
    Levophacetoperane hydrochloride Inhibitor
    Levophacetoperane竞争性抑制去甲肾上腺素 (norepinephrin) 摄取和多巴胺 (dopamine) 摄取。
  • HY-101612
    SPD-473 citrate Inhibitor
    SPD-473 citrate 是 5-HT/多巴胺/去甲肾上腺素再摄取抑制剂。
  • HY-16736
    Centanafadine Inhibitor
    Centanafadine 是去甲肾上腺素 (NE)/多巴胺 (DA) 转运的双抑制剂,还能抑制5-羟色胺 (serotonin) 转运体,其对人 NE,DA 和5-羟色胺转运体的IC50 值分别为6 nM,38 nM 和 83 nM。
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