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.
- A3131 A 438079 hydrochlorideSummary: P2X7 receptor antagonist,competitive and selective
- A3134 A-317491Summary: P2X3 and P2X2/3 receptor antagonist
- A3142 Acamprosate calciumSummary: GABA receptor agonist and modulator of glutamatergic systems
- A3176 AmpalexTarget: AMPA ReceptorsSummary: Ampakine and nootropic
- A3185 AR-C155858Target: Monocarboxylate transporters (MCTs)Summary: MCT1 and MCT2 inhibitor
- A3242 BitopertinSummary: Glycine reuptake inhibitor(GlyT1)
- A3279 CapsazepineSummary: TRPV1 ion channel antagonist
- A3399 Esomeprazole Magnesium trihydrateSummary: Proton pump inhibitor
- A3401 Etifoxine hydrochlorideTarget: GABAA receptorSummary: GABAA receptor potentiator
- A3418 Flecainide acetateTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Antiarrhythmic drug