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.
- B6282 SKF 97541Summary: GABAB agonist
- B6285 3-Methyl-GABASummary: GABA aminotransferase activator
- B6291 β-CCBSummary: benzodiazepine receptor ligand
- B6295 YS-035 hydrochlorideSummary: inhibitor of outward K+ currents
- B6341 trans-4-Hydroxycrotonic acidSummary: ligand of γ-hydroxybutyric acid (GHB) receptor
- A8208 Tariquidar2 CitationTarget: P-glycoprotein (P-gp)Summary: P-glycoprotein inhibitor,potent and non-competitive
- A2700 10Panx1 CitationTarget: Gap JunctionsSummary: Panx-1 mimetic inhibitor
- A2701 Scrambled 10PanxSummary: Panx-1 mimetic inhibitory peptide, blocks pannexin-1 gap junctions
- A3100 (+)-MK 801Target: NMDA ReceptorsSummary: Potent NMDA antagonist
- A3130 A 438079Summary: P2X7 receptor antagonist,competitive and selective