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.
-
B7582 ATPγS tetralithium saltSummary: P2 purinergic receptor agonist -
B6223 Homoquinolinic acidSummary: NMDA receptor agonist -
B6811 IEM 1460Summary: AMPA receptors blocker -
B7389 EIPA3 CitationTarget: Na /H Exchangers (NHEs)Summary: TRPP3 channel inhibitor -
B5740 NS 6180Summary: KCa3.1 channel blocker -
B5765 PF 04885614Summary: NaV1.8 inhibitor -
B1867 Verapamil HCl1 CitationTarget: Voltage-gated Calcium Channels (CaV)Summary: L-type calcium channel blocker -
B6230 Isoguvacine hydrochlorideSummary: GABAA receptor agonist -
B6219 cis-ACPDSummary: NMDA receptor agonist and group II mGluR agonist -
B6781 (S)-CPW 399Summary: AMPA agonist,subtype-selective,weakly desensitizing
