Membrane Transporter/Ion Channel
Ion channels are pore-forming membrane proteins which allow the flow of ions across the membrane. The ion channels can be broadly grouped into six families including calcium channels, chloride channels, potassium channels, sodium channels, gap junction proteins and porins. Not all ion channels are gated, such as certain type of K+ and Cl– channels, transient receptor potential superfamily of cation channels, the ryanodine receptors and the IP3 receptors, but most Na+, K+, Ca2+ and some Cl– channels are all gated by voltage. Ligand-gated channels are regulated in response to ligand binding (e.g. neurotransmitters signaling). These ligand-gated neurotransmitter receptors are known as ionotropic receptors. Various neurotransmitters couple to ionotropic receptors such as glutamate, acetylcholine, glycine, GABA, and serotonin.
- B5312 PPDASummary: Subtype-selective NMDA receptor antagonist
- B5313 TFB-TBOASummary: glial glutamate transporter EAAT1 and EAAT2 inhibitor
- B5350 PEPASummary: Novel allosteric potentiator of AMPA receptor desensitization
- B5410 AZ 10606120 dihydrochlorideTarget: P2X ReceptorsSummary: Potent P2X7 receptor antagonist
- B5439 N2-Methyl-L-arginineSummary: Selective L-arginine uptake inhibitor
- B5463 UBP 310Summary: GLUK5 kainate receptor antagonist
- B5482 MRK 016Summary: GABAA receptor inverse agonist
- B5493 S 18986Summary: positive allosteric modulator of AMPA receptors
- B5499 TCS 1105Summary: GABAA benzodiazepine receptor (BZR) ligand
- B5535 TCN 201Summary: NR1/NR2A selective NMDA receptor antagonist