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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A3699 PAP-1Summary: Kv1.3 inhibitor
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A3758 Retigabine dihydrochlorideSummary: Antiepileptic compound
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A3783 S0859Summary: NBC inhibitor,potent and selective
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A3784 SafinamideSummary: MAO-B inhibitor
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A3809 SDZ 220-581Summary: NMDA glutamate receptor subtype antagonist
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A3811 SEA04004 CitationTarget: Na /Ca2 Exchangers (NCXs)Summary: Specific inhibitor of Na+/Ca2+ exchange
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A3859 Tariquidar methanesulfonate, hydrateTarget: P-glycoprotein (P-gp)Summary: P-glycoprotein inhibitor, potent and selective
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A3899 UK-50991 CitationTarget: Monocarboxylate transporters (MCTs)|mitochondrial pyruvate carrier (MPC)Summary: MCTs and MPC inhibitor
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A3915 Vernakalant HydrochlorideSummary: Ion channel blocker,investigational antiarrhythmic
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A3956 ZosuquidarTarget: P-glycoprotein (P-gp)|Cytochrome P450 (CYP450)Summary: MDR modulator