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(155)
- GC13779Orphenadrine CitrateCAS: 4682-36-4纯度: >98.00%
Orphenadrine citrate 是一种具有口服活性且非竞争性的 NMDA 受体拮抗剂(穿过血脑屏障),Ki 为 6.0 μM。
- GC14533Kynurenic acidCAS: 492-27-3纯度: >99.00% / >98.00%
Kynurenic acid 是一种内源性色氨酸代谢物,是一种针对 NMDA、谷氨酸、α7 烟碱乙酰胆碱受体的广谱拮抗剂。
- GC14842GYKI 53655 hydrochlorideCAS: 143692-48-2纯度: >98.00%
GYKI 53655 (LY300168) hydrochloride 是一种 α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) 拮抗剂。
- GC15363Felbamate hydrateCAS: 1177501-39-1
An inhibitor of NMDA receptors and a modulator of GABA A receptors
- GC16986SDZ 220-581 hydrochlorideCAS: 179411-93-9纯度: >99.50%
SDZ 220-581 hydrochloride 是一种口服有效的竞争性 NMDA 受体拮抗剂,pKi 值为 7.7。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC13684 | S 18986 | 175340-20-2 | - | |
A positive allosteric modulator of AMPA receptors | ||||
| GC13728 | SYM 2206 | 173952-44-8 | >99.50% | |
SYM 2206 是一种有效的非竞争性 AMPA 受体拮抗剂,IC50 为 1.6 μM。 | ||||
| GC13779 | Orphenadrine Citrate | 4682-36-4 | >98.00% | |
Orphenadrine citrate 是一种具有口服活性且非竞争性的 NMDA 受体拮抗剂(穿过血脑屏障),Ki 为 6.0 μM。 | ||||
| GC14039 | MDL-29951 | 130798-51-5 | >99.50% | |
An NMDA receptor antagonist and GPR17 agonist | ||||
| GC14121 | GLYX 13 | 117928-94-6 | - | |
A partial agonist of the NMDA receptor | ||||
| GC14156 | NBQX | 118876-58-7 | >98.50% / >98.00% | |
NBQX是一种高度选择性和竞争性的AMPA受体拮抗剂。 | ||||
| GC14414 | CIQ | 486427-17-2 | >98.00% | |
A subunit-selective NMDA receptor potentiator | ||||
| GC14492 | PF 4778574 | 1219633-99-4 | - | |
PF 4778574 是 AMPA 受体的正向变构调节剂,在不同细胞中的 EC50 为 45 至 919 nM。 | ||||
| GC14495 | CX 546 | 215923-54-9 | >99.00% | |
CX 546是一种强效的3-羟基-5-甲基-4-异唑丙酸(AMPA)受体激活剂,EC 50 值为93.2μM。 | ||||
| GC14533 | Kynurenic acid | 492-27-3 | >99.00% / >98.00% | |
Kynurenic acid 是一种内源性色氨酸代谢物,是一种针对 NMDA、谷氨酸、α7 烟碱乙酰胆碱受体的广谱拮抗剂。 | ||||
| GC14547 | Quinolinic acid | 89-00-9 | >99.00% | |
An excitotoxic agonist at NMDA receptors | ||||
| GC14810 | L-701,324 | 142326-59-8 | >99.50% | |
An NMDA receptor antagonist | ||||
| GC14842 | GYKI 53655 hydrochloride | 143692-48-2 | >98.00% | |
GYKI 53655 (LY300168) hydrochloride 是一种 α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) 拮抗剂。 | ||||
| GC15343 | Eliprodil | 119431-25-3 | >98.50% | |
An NMDA receptor antagonist | ||||
| GC15363 | Felbamate hydrate | 1177501-39-1 | - | |
An inhibitor of NMDA receptors and a modulator of GABA A receptors | ||||
| GC16101 | SYM 2081 | 31137-74-3 | - | |
SYM 2081 是一种高亲和力配体和有效的红藻氨酸受体激动剂,抑制 [3H]-红藻氨酸结合,IC50 为 35 nM,对红藻氨酸受体的选择性分别是 AMPA 和 NMDA 受体的近 3000 倍和 200 倍[1 ]。 | ||||
| GC16149 | Topiramate | 97240-79-4 | >98.00% | |
Topiramate是一种口服有效的磺胺衍生单糖,具有广谱抗癫痫活性。 | ||||
| GC16300 | ZK 200775 | 161605-73-8 | >99.00% | |
ZK 200775 (ZK200775) 是一种高度选择性的 AMPA/红藻氨酸拮抗剂,对 NMDA 几乎没有活性; Ki 值分别为 3.2 nM、100 nM 和 8.5 μ;M 分别针对 quisqualate、红藻氨酸和 NMDA。 | ||||
| GC16315 | D-AP5 | 79055-68-8 | >98.00% | |
D-AP5是一种选择性N-甲基-D-天门冬胺酸(NMDA)受体拮抗剂,K d 值为1.4μM。 | ||||
| GC16562 | PEAQX | 459836-30-7 | >98.00% | |
PEAQX是一种强效且有口服活性的NMDA受体拮抗剂,对hNMDA 1A/2A和1A/2B受体的IC 50 值分别为0.270μM和29.6μM。 | ||||
| GC16776 | QNZ 46 | 1237744-13-6 | >98.00% | |
An antagonist of NR2C- and NR2D-subunit containing NMDA receptors | ||||
| GC16899 | Coluracetam | 135463-81-9 | >98.00% | |
An Analytical Reference Standard | ||||
| GC16986 | SDZ 220-581 hydrochloride | 179411-93-9 | >99.50% | |
SDZ 220-581 hydrochloride 是一种口服有效的竞争性 NMDA 受体拮抗剂,pKi 值为 7.7。 | ||||
| GC17456 | NMDA (N-Methyl-D-aspartic acid) | 6384-92-5 | >98.00% | |
An excitatory neurotransmitter | ||||
