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TargetMol产品目录中 "memantine"的结果
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TargetMol产品目录中 "

memantine

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    TargetMol | Inhibitors_Agonists
  • Memantine
    T2099319982-08-2
    Memantine 是口服具有活性的、非竞争性的N-甲基-D-天冬氨酸受体拮抗剂,可用于研究中重度阿尔茨海默病。
    • ¥ 142
    In stock
    规格
    数量
  • Memantine hydrochloride
    盐酸美金刚, Namenda, Memantine HCl, D-145 (hydrochloride), 3,5-二甲基金刚胺盐酸盐
    T144341100-52-1
    Memantine hydrochloride (Memantine HCl) 是一种具有一些多巴胺能作用的金刚烷胺衍生物,是一种温和的 NMDA 受体非竞争性拮抗剂,能够抑制 CYP2B6 和 CYP2D6。它可作为抗帕金森剂。
    • ¥ 331
    In stock
    规格
    数量
  • Memantine Related Compound B
    美金刚杂质B, 3,5-Dimethyl-1-adamantanol
    T0535707-37-9
    Memantine Related Compound B (3,5-Dimethyl-1-adamantanol) 是Memantine 的杂质。
    • ¥ 173
    待询
    规格
    数量
  • Fluoroethylnormemantine hydrochloride
    T391191639210-25-5
    Fluoroethylnormemantine hydrochloride, a Memantine derivative, functions as an antagonist for the N-methyl-D-aspartate (NMDA) receptor. It can also serve as a positron emission tomography (PET) tracer, specifically as [18F]-Fluoroethylnormemantine hydrochloride. Notably, this compound displays a range of effects, including anti-amnesic, neuroprotective, antidepressant-like, and fear-attenuating properties.
    • ¥ 2990
    5日内发货
    规格
    数量
  • Fluoroethylnormemantine
    T391201639210-26-6
    Fluoroethylnormemantine, a derivative of Memantine, acts as an N-methyl-D-aspartate (NMDA) receptor antagonist. It can function as a positron emission tomography (PET) tracer, known as [18F]-fluoroethylnormemantine. This compound displays anti-amnesic, neuroprotective, antidepressant-like, and fear-attenuating properties.
    • 待询
    5日内发货
    规格
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  • Neramexane Free Base
    T69814219810-59-0
    Neramexane Free Base is a drug related to memantine, which acts as an NMDA antagonist and has neuroprotective effects. It is being developed for various possible applications, including treatment of tinnitus, Alzheimer's disease, drug addiction and as an analgesic.
    • ¥ 10600
    1-2周
    规格
    数量
  • AChE-IN-41
    T83187
    AChE-IN-41(Compound 2)是一种加兰他敏-美金刚杂交体化合物,能够抑制胆碱酯酶。在体外,该化合物展现出较高的血浆稳定性和良好的微粒体稳定性;而在体内,则具有较短的半衰期和较快的清除速率。
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