目录号 | 产品详情 | 靶点 | |
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T80210 | DAPK | ||
TAT-GluN2BCTM 是一种靶向DAPK1的膜透性肽,能够促使活性DAPK1定向降解于溶酶体。该化合物通过降低DAPK1的表达,有助于防护神经元免遭氧化应激和NMDAR-介导的兴奋毒性。TAT-GluN2BCTM常用于神经保护性研究领域。 | |||
T82528 | |||
DQP-997-74(compound 2i)是一种针对NMDAR的选择性抑制剂,GluN2C/D的IC50分别为0.069 μM和0.035 μM,显示出良好的血脑屏障透过性。DQP为二氢喹啉-吡唑啉。该化合物能够在激动剂谷氨酸的作用下,表现出对高频兴奋性突触传递所驱动的超同步活动具有时间依赖性的增强抑制作用。在TSC诱导的癫痫小鼠模型中,DQP-997-74有效减少了发作次数,适用于NMDAR相关神经系统疾病的研究。 | |||
T76250 | |||
VSGLNPSLWSIFGLQFILLWLVSGSRHYLW 是一种由 30 个氨基酸构成的肽,用于模拟 α2δ-1 的 C 端结构域。该化合物能够有效地在体内外阻断 α2δ-1 与 NMDAR 的相互作用,适用于神经性疼痛的研究。 | |||
T76250L | |||
VSGLNPSLWSIFGLQFILLWLVSGSRHYLW (TFA) 是一种模拟 α2δ-1 的 C 端结构域的肽,由 30 个氨基酸组成。该化合物能够在体内外有效阻断 α2δ-1 与 NMDAR 的相互作用,适用于神经性疼痛的研究。 | |||
T8435 | GluR iGluR | ||
YM90K (6-(1H-imidazol-1-yl)-7-nitro-2,3(1H,4H)-) hydrochloride 是一种选择性的、有效的AMPA 受体拮抗剂,Ki=84 nM。YM90K 抑制海藻酸酯 (Ki 为 2.2 μM) 和 NMDA (Ki 为 37 μM) 受体的效力较低,并具有神经保护活性。 | |||
T73359 | |||
NYX-2925 是一种口服有效的NMDAR 调节剂。NYX-2925 恢复 mPFC 中 GluN2A 和 GluN2B 上活化的Src 和Src 磷酸化位点的水平。NYX-2925 对 CAMKII 没有影响,也没有任何成瘾或镇静/共济失调的副作用。NYX-2925 可用于多种 NMDA 受体介导的中枢神经系统疾病的研究。 | |||
T76069 | |||
Tat-NR2BAA TFA 是 Tat-NR2B9c 的对照肽 (control peptide),没有活性。Tat-NR2BAA TFA 的序列与 Tat-NR2B9c 相似,但在 COOH 末端 tSXV 基序中有一个双点突变,这使得它无法结合 PSD-95。Tat-NR2B9c TFA 是一种可通透细胞膜的多肽,破坏 PSD-95/NMDAR 的结合。 | |||
T0802 | Histone Demethylase 5-HT Receptor DNA/RNA Synthesis Sodium Channel NMDAR AChR | ||
Procaine hydrochloride (Novocaine HCl) 是DNA 脱甲基剂,是一种苯甲酸衍生物,具有局部麻醉和抗心律失常特性。 | |||
T35924 | |||
Tat-NR2BAA is an inactive control peptide of Tat-NR2B9c. It shares a similar sequence with Tat-NR2B9c, but possesses a double-point mutation in the COOH terminal tSXV motif. This mutation renders Tat-NR2BAA unable to bind PSD-95. Tat-NR2B9c, on the other hand, is a membrane-permeable peptide that interferes with PSD-95/NMDAR binding. This interference leads to the decoupling of NR2B- and/or NR2A-type NMDARs from PSD-95[1][2]. | |||
T0051 | Chloride channel GABA Receptor Antibacterial GluR NMDAR AChR Parasite | ||
Urethane (Ethylurethane) 是多种食品中发酵形成的副产物,是氨基甲酸的乙酯,具有抑制细菌、海胆卵、原生动物和植物组织生长的作用。 |
目录号 | 产品名/同用名 | 种属 | 表达系统 | ||
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TMPY-01692 | NETO1 Protein, Human, Recombinant (His) | Human | HEK293 | ||
Neuropilin tolloid-like 1 (NETO1), a complement C1r/C1s, Uegf, Bmp1 (CUB) domain-containing transmembrane protein, is a novel component of the NMDAR complex critical for maintaining the abundance of NR2A-containing NMDARs in the postsynaptic density. The N-methyl-D-aspartate receptor (NMDAR), a major excitatory ligand-gated ion channel in the central nervous system (CNS), is a principal mediator of synaptic plasticity. Both NETO1 and NETO2 share an identical and unique domain structure thus representing a novel subfamily of CUB- and LDLa-containing proteins. The cytoplasmic domains of NETO1 and NETO2 are not homologous to other known protein sequences but contain a conserved FXNPXY-like motif, which is essential for the internalization of clathrin-coated pits during endocytosis or may be implicated in intracellular signaling pathways. NETO1 and NETO2, have marked effects on receptor properties, increasing further the potential diversity of Kainate receptors (KARs) functional properties. NETO1 involves in the development and/or maintenance of neuronal circuitry. NETO1 regulates long-term NMDA receptor-dependent synaptic plasticity and cognition, at least in the context of spatial learning and memory.
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TMPY-02750 | Neuroligin-1 Protein, Mouse, Recombinant (His) | Mouse | HEK293 | ||
Neuroligin 1 (NLGN1) belongs to the type-B carboxylesterase/lipase family, is a synaptic cell-adhesion molecule that is enriched in postsynaptic densities where it may recruit receptors, channels, and signal-transduction molecules to synaptic sites of cell adhesion. Neuroligins consists of five members (NLGN1, NLGN2, NLGN3, NLGN4, and NLGN4Y), which interact with beta-neurexins, and this interaction is involved in the formation of functional synapses. The extracellular domain of functional Neuroligin 1 associates as a dimer when analyzed by sedimentation equilibrium. Neuroligin 1 has a unique N-linked glycosylation pattern in the neuroligin family, and glycosylation and its processing modify neuroligin activity. Neuroligin 1 is a potent trigger for the de novo formation of synaptic connections, and it has recently been suggested that it is required for the maturation of functionally competent excitatory synapses. The persistent expression of Neuroligin 1 is required for the maintenance of NMDAR-mediated synaptic transmission, which enables the normal development of synaptic plasticity and long-term memory in the amygdala of adult animals.
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TMPY-01726 | Neuroligin-1 Protein, Human, Recombinant (His) | Human | HEK293 | ||
Neuroligin 1 (NLGN1) belongs to the type-B carboxylesterase/lipase family, is a synaptic cell-adhesion molecule that is enriched in postsynaptic densities where it may recruit receptors, channels, and signal-transduction molecules to synaptic sites of cell adhesion. Neuroligins consists of five members (NLGN1, NLGN2, NLGN3, NLGN4, and NLGN4Y), which interact with beta-neurexins, and this interaction is involved in the formation of functional synapses. The extracellular domain of functional Neuroligin 1 associates as a dimer when analyzed by sedimentation equilibrium. Neuroligin 1 has a unique N-linked glycosylation pattern in the neuroligin family, and glycosylation and its processing modify neuroligin activity. Neuroligin 1 is a potent trigger for the de novo formation of synaptic connections, and it has recently been suggested that it is required for the maturation of functionally competent excitatory synapses. The persistent expression of Neuroligin 1 is required for the maintenance of NMDAR-mediated synaptic transmission, which enables the normal development of synaptic plasticity and long-term memory in the amygdala of adult animals.
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