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.
- B6787 STO-609 acetateTarget: CaM-KKSummary: Ca2+-calmodulin-dependent protein kinase kinase inhibitor
- B7182 Philanthotoxin 74Summary: AMPA receptor antagonist
- B5124 LY 233053Summary: Competitive NMDA receptor antagonist
- B6205 D-AP5Summary: NMDA antagonist
- B7786 TRAM 39Summary: Potent KCa3.1 blocker
- B7789 Huwentoxin XVISummary: N-type Ca2+ channel blocker,potent and selective
- A8896 (+)-MK 801 MaleateSummary: Potent NMDA antagonist
- B4798 Procainamide HClTarget: DNA MethyltransferasesSummary: sodium channel blocker
- B4884 RBC8Summary: Ral GTPase inhibitor
- B4849 AzimilideSummary: class III anti-arrhythmic drug