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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A3399 Esomeprazole Magnesium trihydrateSummary: Proton pump inhibitor
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B1388 Esomeprazole SodiumSummary: Proton pump inhibitor
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B2201 Zinc PyrithioneTarget: Proton PumpSummary: Proton pump inhibitor
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B2200 Esomeprazole MagnesiumSummary: Proton pump inhibitor
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B1290 Lansoprazole sodiumSummary: PPI/cytochrome P450 inhibitor
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A1229 LansoprazoleSummary: H+,K+-ATPase inhibitor
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B5439 N2-Methyl-L-arginineSummary: Selective L-arginine uptake inhibitor
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B3466 Rabeprazole sodiumSummary: proton pump inhibitor
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B3467 RabeprazoleSummary: proton pump inhibitor
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B4720 PantoprazoleSummary: H+/K+-ATPase inhibitor