1. Signaling Pathways
  2. Membrane Transporter/Ion Channel
    Neuronal Signaling
  3. iGluR

iGluR (离子型谷氨酸受体)

Ionotropic glutamate receptors

iGluR(离子型谷氨酸受体)是一种配体门控离子通道,由神经递质谷氨酸激活。iGluR 是整合膜蛋白,由四个大亚基组成,形成一个中央离子通道孔。所有已知的谷氨酸受体亚基之间的序列相似性,包括 AMPA、海人酸、NMDA 和 δ 受体。

AMPA 受体是基础传递过程中的主要电荷载体,允许钠离子流入以使突触后膜去极化。NMDA 受体被镁离子阻断,因此只允许在先前去极化后离子通量。这使它们能够充当突触可塑性的巧合检测器。通过 NMDA 受体的钙流入导致突触传递强度的持续改变。

iGluR (ionotropic glutamate receptor) is a ligand-gated ion channel that is activated by the neurotransmitter glutamate. iGluR are integral membrane proteins compose of four large subunits that form a central ion channel pore. Sequence similarity among all known glutamate receptor subunits, including the AMPA, kainate, NMDA, and δ receptors.

AMPA receptors are the main charge carriers during basal transmission, permitting influx of sodium ions to depolarise the postsynaptic membrane. NMDA receptors are blocked by magnesium ions and therefore only permit ion flux following prior depolarisation. This enables them to act as coincidence detectors for synaptic plasticity. Calcium influx through NMDA receptors leads to persistent modifications in the strength of synaptic transmission.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-119776
    UBP618 Inhibitor
    UBP618 是一种非选择性 N-methyl-D-aspartate 抑制剂。
    UBP618
  • HY-164264
    Caged MK801 Inhibitor
    Caged MK801 (cMK801) 是选择性的、非竞争性的,不可逆的 NMDA 受体开放通道的阻断剂。NVOC笼在神经药理学上是相容的,不改变分子本身活性。
    Caged MK801
  • HY-167885
    SN-35210 free base Inhibitor
    SN-35210 (free base) 是一种氯胺酮酯类类似物,通过酯酶介导的水解作用实现快速消除。
    SN-35210 free base
  • HY-112699
    AMPA receptor modulator-1 Inhibitor
    AMPA receptor modulator-1 是一种口服有效的选择性 AMPAR 调控蛋白 TARP γ-8 的负调节剂,pIC50 值为 9.7,对其选择性远高于 GluA1/γ-2 (pIC50=5)。
    AMPA receptor modulator-1
  • HY-P1594
    Dynorphin A (1-10) Inhibitor
    Dynorphin A (1-10) 是一种内源性的阿片样神经肽,与 κ 阿片受体 (κ-opioid receptor) 结合。Dynorphin A (1-10) 也阻断 NMDA 激活的电流,IC50 为 42.0 μM。
    Dynorphin A (1-10)
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