1. Signaling Pathways
  2. Membrane Transporter/Ion Channel
  3. Monoamine Transporter

Monoamine Transporter (单胺转运蛋白)

Monoamine transporters (MATs) belong to the solute carrier 6 (SLC6) family of human transporters, which, in turn, is a subfamily of the broader neurotransmitter:sodium symporters (NSSs) that comprise transporters from prokaryotic to human. MATs comprise three main members-the dopamine (DA) transporter (DAT), serotonin transporter (SERT) and norepinephrine transporter (NET). MATs regulate neurotransmission via the reuptake of dopamine, serotonin and norepinephrine from extra-neuronal regions and thus maintain neurotransmitter homeostasis.

MATs are transmembrane proteins located in plasma membranes of monoaminergic neurons. These proteins use ion (Na+, Cl) gradients as energy sources to move monoamines into or out of neurons. In the membrane of intracellular synaptic vesicles is the vesicular monoamine transporters 1 and 2 (VMAT1 and VMAT2), which use a proton gradient as the energy source to sequester cytosolic monoamines into the vesicles and then release the monoamines into synaptic cleft by exocytosis. Dysregulation of MATs has been linked to depression, anxiety disorder, attention-deficit-hyperactivity disorder, obsessive-compulsive disorder, substance-use disorders, epilepsy, Parkinson’s disease and autism-spectrum disorder. Thus, MATs serve as pharmacological targets for several neuropsychiatric and neurodegenerative disorders.

Monoamine Transporter 相关产品 (30):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N7506
    13-Hydroxyisobakuchiol Inhibitor
    13-Hydroxyisobakuchiol (Delta3,2-Hydroxylbakuchiol) 是从 Psoralea corylifolia 中分离得到,Bakuchiol (HY-N0235) 的类似物。13-Hydroxyisobakuchiol 是一种有效的单胺转运蛋白 (monoamine transporter) 抑制剂,它对多巴胺转运蛋白 (DAT) (IC50=0.58 μM) 和去甲肾上腺素转运蛋白 (NET) (IC50=0.69 μM) 的选择性比血清素转运蛋白 (SERT) (IC50=312.02 μM) 更强。13-Hydroxyisobakuchiol 有潜力用于帕金森病和抑郁症等疾病的研究。
    13-Hydroxyisobakuchiol
  • HY-153472
    VMAT2-IN-2 tosylate Inhibitor
    VMAT2-IN-2 tosylate 是一种有效的 VMAT2 抑制剂。VMAT2-IN-2 tosylate 可用于迟发性运动障碍的研究。
    VMAT2-IN-2 tosylate
  • HY-16771A
    Valbenazine tosylate Inhibitor
    Valbenazine tosylate (NBI-98854 tosylate) 是一种囊泡单胺类转运 2 (VMAT2) 抑制剂,Ki 为 110-190 nM。
    Valbenazine tosylate
  • HY-148863
    Cavα2δ1&NET-IN-2 Inhibitor
    Cavα2δ1&NET-IN-2 (Compound 45CS) 是电压门控钙通道 α2δ-1 亚单位 (Cavα2δ-1) 和去甲肾上腺素转运蛋白 (NET) 的双重抑制剂。Cavα2δ1&NET-IN-2 抑制 Cavα2δ-1 的 Ki 为 454 nM。Cavα2δ1&NET-IN-2 抑制 NET 的 Ki 为 59 nM,IC50 为 7 nM。Cavα2δ1&NET-IN-2 可用于疼痛研究。
    Cavα2δ1&NET-IN-2
  • HY-15793A
    Trans (2,3)-Dihydrotetrabenazine

    顺式(2R,3R,11bR)-二式(2R,3R,11bR)-二氢丁苯那嗪

    Inhibitor
    Trans (2,3)-Dihydrotetrabenazine ((2R,3R,11bR)-rel-Dihydrotetrabenazine), 是抗精神病活性分子Tetrabenazine的体内代谢物,能够抑制囊泡单胺转运体 2 (VMAT2)
    Trans (2,3)-Dihydrotetrabenazine
  • HY-137107
    Radafaxine Inhibitor
    Radafaxine ((S,S)-Hydroxybupropion) 是一种抗抑郁化合物。 Radafaxine 阻断多巴胺转运蛋白 (DAT)。 Radafaxine 是安非他酮的活性代谢物。
    Radafaxine
  • HY-G0025
    Tetrabenazine Metabolite Inhibitor
    Tetrabenazine Metabolite ((-)-β-Dihydrotetrabenazine) 是 Tetrabenazine 的一种活性代谢物。Tetrabenazine Metabolite 是一种囊泡单胺转运蛋白 2 (VMAT2) 抑制剂。对 VMAT2 具有高亲和力,Ki=13.4 nM。Tetrabenazine Metabolite 可用于研究与亨廷顿氏病和其他多动障碍相关的舞蹈病。
    Tetrabenazine Metabolite
  • HY-148862
    Cavα2δ1&NET-IN-1 Inhibitor
    Cavα2δ1&NET-IN-1 (Compound 59S) 是电压门控钙通道 α2δ-1 亚单位 (Cavα2δ-1) 和去甲肾上腺素转运蛋白 (NET) 的双重抑制剂。Cavα2δ1&NET-IN-1 抑制 Cavα2δ-1 的 Ki 为 112 nM。Cavα2δ1&NET-IN-1 抑制 NET 的 Ki 为 383 nM,IC50 为 67 nM。Cavα2δ1&NET-IN-1 可用于疼痛研究。
    Cavα2δ1&NET-IN-1
  • HY-103465
    FFN511 Inhibitor
    FFN511 是一种靶向神经元囊泡单胺转运体 2 (VMA T2) 的荧光假神经递质 (FFNs)。FFN511 可抑制 5-羟色胺与含 VMA T2 的膜结合,其 IC50 值为 1 µM。FFN511 能直接反映细胞外渗过程中的释放动态,可用于标记活体皮质-纹状体急性切片中的多巴胺能神经末梢。
    FFN511
  • HY-B0590S1
    (+)-Tetrabenazine-d6

    (+)-丁苯那嗪 d6; (+)-丁苯喹嗪 d6; (+)-特苯那嗪 d6; (+)-四苯喹嗪 d6

    (+)-Tetrabenazine-d6 是 (+)-Tetrabenazine 的氘代物。(+)-Tetrabenazine 是一种不可逆的 vesicular monoamine transporter 2 抑制剂。
    (+)-Tetrabenazine-d<sub>6</sub>