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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B6291 β-CCBSummary: benzodiazepine receptor ligand -
B7154 YM 90K hydrochlorideSummary: AMPA receptor antagonist -
B7520 BCTCSummary: vanilloid receptor 1 (TRPV1 receptor) antagonist -
B5927 GSK1014802(CNV1014802)Summary: Novel sodium channel blocker -
B6239 ACBCSummary: NMDA receptor partial agonist -
B5048 ω-Conotoxin GVIASummary: blocker of N-type calcium channels -
B6285 3-Methyl-GABASummary: GABA aminotransferase activator -
B6295 YS-035 hydrochlorideSummary: inhibitor of outward K+ currents -
B7103 GYKI 53655 hydrochlorideSummary: AMPA and kainate receptor antagonist -
B7494 Pyr3Summary: canonical transient receptor potential channel 3 (TRPC3) antagonist
