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.
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B7573 SipatrigineSummary: voltage-dependent sodium channels (NaV) blocker -
B5622 ML 218 hydrochlorideSummary: T-type calcium channels inhibitor -
C5065 GSK1016790ASummary: TRPV4 agonist -
B6287 Arcaine sulfateSummary: NMDA antagonist -
B6460 THIP hydrochlorideSummary: GABAA receptor agonist and GABAA-ρ receptor antagonist -
B6711 CromakalimSummary: Kir6 (KATP) channel opener -
B7569 Ralfinamide mesylateSummary: Sodium channel blocker -
B7613 IEM 1925 dihydrobromideSummary: AMPA receptor antagonist -
B7512 NPEC-caged-(S)-AMPASummary: AMPA receptor agonist -
B5501 cis-Ned 19Summary: nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist
