iGluR
iGluR(离子型谷氨酸受体)
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.
iGluR 相关产品(156)
- GA10750L-Glutamic acidCAS: 56-86-0纯度: >99.00%
L-Glutamic acid是哺乳动物中枢神经系统(CNS)中的主要兴奋性神经递质。L-Glutamic acid有两种主要类型的受体:离子型(NMDA-, AMPA- and kainate-selective iGluRs)和代谢型谷氨酸受体。L-Glutamic acid对突触后N-甲基-D-天冬氨酸受体的激动作用产生兴奋毒性,从而导致神经退行性病变。
- GC10198Memantine hydrochlorideCAS: 41100-52-1纯度: >98.00%
Memantine hydrochloride是一种非竞争性N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂,IC 50 值为0.5-1μM。
- GC107817-Chlorokynurenic acidCAS: 18000-24-3纯度: >99.50%
A glycine-site selective NMDA receptor antagonist
- GC113957-Chlorokynurenic acid sodium saltCAS: 1263094-00-3纯度: >99.50%
A glycine-site selective NMDA receptor antagonist
- GC11585TCN 237 dihydrochlorideCAS: 700878-19-9纯度: >98.00%
TCN 237 dihydrochloride 是一种有效的 NR2B 选择性 NMDA 拮抗剂,Ki 为 0.85 nM; NR2B Ca2+ 内流 IC50 为 9.7 nM;对 NR2A、NR2C、NR2D、hERG 通道和 α1-肾上腺素能受体无活性。
- GC11715Ibotenic acidCAS: 2552-55-8纯度: >99.00% / >98.00%
Ibotenic acid是一种神经毒素,对N-甲基-D-天冬氨酸(NMDA)和反式ACPD或代谢使君子酸(Qm)受体位点均具有激动剂活性。
- GC11889(S)-(-)-5-FluorowillardiineCAS: 140187-23-1纯度: >95.00%
(S)-(-)-5-Fluorowillardiine 是一种有效且特异性的 AMPAR 激动剂。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GA10750 | L-Glutamic acid | 56-86-0 | >99.00% | |
L-Glutamic acid是哺乳动物中枢神经系统(CNS)中的主要兴奋性神经递质。L-Glutamic acid有两种主要类型的受体:离子型(NMDA-, AMPA- and kainate-selective iGluRs)和代谢型谷氨酸受体。L-Glutamic acid对突触后N-甲基-D-天冬氨酸受体的激动作用产生兴奋毒性,从而导致神经退行性病变。 | ||||
| GA10922 | H-Gly-OH | 56-40-6 | >99.00% / >99.50% | |
H-Gly-OH 是 CNS 中的一种抑制性神经递质,还与谷氨酸一起作为共激动剂,促进谷氨酰胺能 N-甲基-D-天冬氨酸 (NMDA) 受体的兴奋电位。 | ||||
| GA11306 | H-D-Ser-OH | 312-84-5 | >99.00% | |
An NMDA co-agonist | ||||
| GA11338 | H-D-Asp-OH | 1783-96-6 | >99.00% | |
An amino acid and a precursor in NMDA biosynthesis | ||||
| GC10198 | Memantine hydrochloride | 41100-52-1 | >98.00% | |
Memantine hydrochloride是一种非竞争性N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂,IC 50 值为0.5-1μM。 | ||||
| GC10270 | Noopept | 157115-85-0 | >99.50% | |
An Analytical Reference Standard | ||||
| GC10443 | Meclofenoxate hydrochloride | 3685-84-5 | >98.00% | |
A nootropic agent | ||||
| GC10522 | Felbamate | 25451-15-4 | >98.00% | |
An inhibitor of NMDA receptors and a modulator of GABA A receptors | ||||
| GC10781 | 7-Chlorokynurenic acid | 18000-24-3 | >99.50% | |
A glycine-site selective NMDA receptor antagonist | ||||
| GC11124 | Lanicemine | 153322-05-5 | >95.00% | |
A low-trapping NMDA channel blocker | ||||
| GC11395 | 7-Chlorokynurenic acid sodium salt | 1263094-00-3 | >99.50% | |
A glycine-site selective NMDA receptor antagonist | ||||
| GC11470 | Flupirtine maleate | 75507-68-5 | >99.50% | |
An activator of Kv7 channels | ||||
| GC11585 | TCN 237 dihydrochloride | 700878-19-9 | >98.00% | |
TCN 237 dihydrochloride 是一种有效的 NR2B 选择性 NMDA 拮抗剂,Ki 为 0.85 nM; NR2B Ca2+ 内流 IC50 为 9.7 nM;对 NR2A、NR2C、NR2D、hERG 通道和 α1-肾上腺素能受体无活性。 | ||||
| GC11715 | Ibotenic acid | 2552-55-8 | >99.00% / >98.00% | |
Ibotenic acid是一种神经毒素,对N-甲基-D-天冬氨酸(NMDA)和反式ACPD或代谢使君子酸(Qm)受体位点均具有激动剂活性。 | ||||
| GC11799 | CNQX | 115066-14-3 | >98.00% | |
CNQX是一种有效的竞争性AMPA /海藻酸酯受体(AMPA/kainate receptor)拮抗剂,IC50 分别为0.3µM和1.5µM。 | ||||
| GC11889 | (S)-(-)-5-Fluorowillardiine | 140187-23-1 | >95.00% | |
(S)-(-)-5-Fluorowillardiine 是一种有效且特异性的 AMPAR 激动剂。 | ||||
| GC12703 | Philanthotoxin 74 | 1227301-51-0 | >98.00% | |
An AMPA receptor antagonist | ||||
| GC12863 | 1-BCP | 34023-62-6 | - | |
A positive allosteric modulator of AMPA receptors | ||||
| GC13007 | PEPA | 141286-78-4 | >99.50% | |
A positive allosteric modulator of AMPA receptors | ||||
| GC13010 | LY451395 | 375345-95-2 | >99.50% | |
LY451395 (LY451395) 是一种有效且高度选择性的 AMPA 受体增强剂。 | ||||
| GC13164 | Ampalex | 154235-83-3 | >99.50% | |
An AMPA receptor modulator | ||||
| GC13290 | CMPDA | 380607-77-2 | - | |
A positive allosteric modulator of GluA2 | ||||
| GC13349 | Naspm trihydrochloride | 1049731-36-3 | >98.00% | |
A synthetic analog of Joro spider toxin | ||||
| GC13469 | Piracetam | 7491-74-9 | >99.00% | |
An Analytical Reference Standard | ||||
