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 (14):

目录号 产品名 作用方式 纯度
  • HY-N0480
    Reserpine Inhibitor
    Reserpine 是囊泡单胺转运蛋白 2 (VMAT2) 的抑制剂。
  • HY-B0590
    Tetrabenazine Inhibitor ≥99.0%
    Tetrabenazine是VMAT抑制剂,可作用于多动性运动障碍。
  • HY-17590
    Radafaxine hydrochloride Inhibitor 99.88%
    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。
  • HY-N0480A
    Reserpine hydrochloride Inhibitor 99.65%
    Reserpine (hydrochloride) 是囊泡单胺转运蛋白 2 (VMAT2) 的抑制剂。
  • HY-15793
    NBI-98782 Inhibitor 99.80%
    NBI-98782(alpha-dihydrotetrabenazine)是囊泡单胺转运体(VMAT2)抑制剂,Ki为0.97nM。
  • HY-131006
    FFN200 dihydrochloride
    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。
  • HY-B0590B
    (+)-Tetrabenazine Inhibitor ≥99.0%
    (+)-Tetrabenazine ((+)-TBZ; (3R,11bR)-TBZ; (3R,11bR)-Tetrabenazine) 是一个可逆转的VMAT-2的抑制剂。
  • HY-B0590A
    Tetrabenazine Racemate 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。
  • HY-B1704A
    Nisoxetine hydrochloride Inhibitor ≥98.0%
    Nisoxetine hydrochloride 是一种有效的和选择性的去甲肾上腺素转运蛋白 (NET) 的抑制剂,Kd 值为 0.76 nM。Nisoxetine hydrochloride 是一种抗抑郁药和局部麻药,它可以阻断电压门控性钠通道。
  • HY-101416
    Vanilpyruvic acid ≥98.0%
    Vanilpyruvic acid是儿茶酚胺代谢物和香草酸的前体。
  • HY-B0590S
    Tetrabenazine D6 Inhibitor ≥99.0%
    Tetrabenazine D6 是Tetrabenazine 的氘代物。
  • 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、抑郁症和可卡因成瘾等疾病的研究。
  • HY-15793A
    Trans (2,3)-Dihydrotetrabenazine Inhibitor
    Trans (2,3)-Dihydrotetrabenazine ((2R,3R,11bR)-rel-Dihydrotetrabenazine), 是抗精神病药物Tetrabenazine的体内代谢物,能够抑制囊泡单胺转运体 2 (VMAT2)
  • HY-B0590S1
    (+)-Tetrabenazine D6
    (+)-Tetrabenazine D6 是 (+)-Tetrabenazine 的氘代物。(+)-Tetrabenazine 是一种不可逆的 vesicular monoamine transporter 2 抑制剂。
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