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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A8524 Sodium OrthovanadateTarget: Protein Tyrosine Phosphatases|alkaline phosphatases|ATPasesSummary: PTP inhibitor
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A8549 LY335979 (Zosuquidar 3HCL)1 CitationTarget: P-glycoprotein (P-gp)Summary: Pgp (P-glycoprotein) inhibitor
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A8553 PTC124 (Ataluren)Summary: CFTR-G542X nonsense allele inhibitor
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A8637 IOWH-032Target: CFTRSummary: CFTR inhibitor
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B3041 BTB06584Target: F1 Fo-ATPaseSummary: F1F0 ATP synthases
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B1055 IcilinTarget: TRP ChannelSummary: TRPM8/ hENaCδ agonist
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B2277 A-803467Target: Voltage-gated Sodium (NaV) ChannelsSummary: NaV1.8 channel blocker,potent and selective
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A3401 Etifoxine hydrochlorideTarget: GABAA receptorSummary: GABAA receptor potentiator
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A3418 Flecainide acetateTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Antiarrhythmic drug
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A3507 Istaroxime1 CitationTarget: Na /K ATPasesSummary: Na+/K+ ATPase inhibitor