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 (39):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N0480
    Reserpine

    利血平

    Inhibitor 99.83%
    Reserpine 是囊泡单胺转运蛋白 2 (VMAT2) 的抑制剂。
    Reserpine
  • HY-B0590
    Tetrabenazine

    丁苯那嗪

    Inhibitor 98.23%
    Tetrabenazine (Ro 1-9569) 是一种可逆的囊泡单胺转运蛋白 VMAT2 位点抑制剂,其 Kd 值为 1.34 nM,可用于亨廷顿舞蹈病等多动性运动障碍相关疾病研究。
    Tetrabenazine
  • HY-16771
    Valbenazine Inhibitor 98.91%
    Valbenazine (NBI-98854) 是一种囊泡单胺类转运 2 (VMAT2) 抑制剂,Ki 为 110-190 nM。
    Valbenazine
  • HY-107740
    Pseudoisocyanine iodide Inhibitor 99.92%
    Pseudoisocyanine (iodide) 是单胺转运体和有机阳离子转运体的泛抑制剂,具有抗抑郁活性。
    Pseudoisocyanine iodide
  • HY-17590
    Radafaxine hydrochloride

    安非他酮杂质

    Inhibitor 99.01%
    Radafaxine hydrochloride (GW-353162A) 是 bupropion 的代谢活化物,DAT/NET 转运体抑制剂,能选择性的抑制去甲肾上腺素的再吸收。
    Radafaxine hydrochloride
  • HY-12798
    Netarsudil Inhibitor
    Netarsudil 是一种 Rho 激酶 (ROCK) 和去甲肾上腺素转运体 (NET) 抑制剂。Netarsudil 通过多种机制增加人眼的流出能力。
    Netarsudil
  • HY-161433
    VMAT2-IN-3 Inhibitor
    VMAT2-IN-3 (compound 10) 是一种有效的囊泡单胺转运蛋白 2 (VMAT2) 抑制剂,Ki 为 0.71 nM。VMAT2-IN-3 具有用于神经或精神疾病研究的潜力。
    VMAT2-IN-3
  • HY-120788
    VMAT2-IN-4 Inhibitor
    VMAT2-IN-4 (compound 11) 是一个 vesicular monoamine transporter-2 (VMAT2) 抑制剂。VMAT2-IN-4 可抑制 [3H]-DTBZ 结合 (Ki = 560 nM)。VMAT2-IN-4 可抑制 [3H]-DA (Ki = 45 nM) 进入囊泡被细胞摄取。VMAT2-IN-4 可用于冰毒成瘾相关研究。
    VMAT2-IN-4
  • HY-N0480A
    Reserpine hydrochloride

    利血平盐酸盐

    Inhibitor 99.90%
    Reserpine (hydrochloride) 是囊泡单胺转运蛋白 2 (VMAT2) 的抑制剂。
    Reserpine hydrochloride
  • HY-B1704A
    Nisoxetine hydrochloride

    盐酸尼索西汀

    Inhibitor 99.81%
    Nisoxetine hydrochloride 是一种有效的和选择性的去甲肾上腺素转运蛋白 (NET) 抑制剂,Kd 值为 0.76 nM。Nisoxetine hydrochloride 是一种抗抑郁试剂和局部麻药,它可以阻断电压门控性钠通道
    Nisoxetine hydrochloride
  • HY-B1704
    Nisoxetine

    尼索西汀

    Inhibitor 98.28%
    Nisoxetine 是一种有效的和选择性的去甲肾上腺素转运蛋白 (NET) 抑制剂,Kd 值为 0.76 nM。Nisoxetine 是一种抗抑郁试剂和局部麻药,它可以阻断电压门控性钠通道
    Nisoxetine
  • HY-B0590A
    Tetrabenazine Racemate

    丁苯那嗪外消旋体

    Inhibitor ≥98.0%
    Tetrabenazine Racemate (Ro 1-9569 Racemate) 是一个有选择性和可逆转的VMAT-2抑制剂。
    Tetrabenazine Racemate
  • HY-101416
    Vanilpyruvic acid

    4-羟基-3-甲氧苯丙酮酸

    98.28%
    Vanilpyruvic acid是儿茶酚胺代谢物和香草酸的前体。
    Vanilpyruvic acid
  • HY-110165
    hENT4-IN-1 Inhibitor 98.14%
    hENT4-IN-1 是一种有效且选择性的人源 ENT4 (平衡核苷转运体 4) 抑制剂,IC50 为 74.4 nM。
    hENT4-IN-1
  • HY-15793
    NBI-98782

    (+)-α-二氢丁苯那嗪

    Inhibitor 98.56%
    NBI-98782 是一种高亲和力和选择性的囊泡单胺转运蛋白 2 (VMAT2) 抑制剂,Ki 为 3 nM。NBI-98782 具有抗精神病活性。
    NBI-98782
  • HY-B0590B
    (+)-Tetrabenazine

    (+)-丁苯那嗪

    Inhibitor ≥98.0%
    (+)-Tetrabenazine ((+)-TBZ; (3R,11bR)-TBZ; (3R,11bR)-Tetrabenazine) 是一个可逆转的VMAT-2的抑制剂。
    (+)-Tetrabenazine
  • HY-117883
    GZ-793A Inhibitor 99.50%
    GZ-793A 是一种具有口服活性和选择性的囊泡单胺转运体-2 (VMAT2) 抑制剂,其 Ki 值为 0.029 µM。GZ-793A 能抑制甲基苯丙胺 (METH) 诱导的多巴胺释放,可用于 METH 成瘾研究。
    GZ-793A
  • HY-B0590S
    Tetrabenazine-d6

    丁苯那嗪 D6

    Inhibitor ≥99.0%
    Tetrabenazine-d6 (Deutetrabenazine) 是 Tetrabenazine (HY-B0590) 的氘代物,是全球首个批准的氘代物,可用于亨廷顿舞蹈症及其他多动运动障碍的研究。
    Tetrabenazine-d<sub>6</sub>
  • HY-149170
    FFN246 99.79%
    FFN246 是 serotonin transporter (SERT) vesicular monoamine transporter 2 (VMAT2) 的荧光双底物探针,激发和发射光谱为 392/427 nm。FFN246 可以通过 SERT 依赖性积累来标记小鼠脑组织中的 5-羟色胺能神经元。
    FFN246
  • HY-131006
    FFN200 dihydrochloride ≥99.0%
    FFN200 dihydrochloride 是 VMAT2 的一个荧光第五,在神经元细胞和脑组织中选择性的微量单胺胞吐。测定FFN200 荧光和发射波长最大值分别为 352 nm 和 451 nm。
    FFN200 dihydrochloride