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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B4798 Procainamide HClTarget: DNA MethyltransferasesSummary: sodium channel blocker
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B4849 AzimilideSummary: class III anti-arrhythmic drug
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B7113 PSB 06126Target: NTPDasesSummary: NTPDase 3 inhibitor
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B7335 SB 452533Target: TRPVSummary: TRPV1 antagonist
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B7388 ValinomycinTarget: IonophoresSummary: potassium-specific transporter
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B7659 Psora 41 CitationTarget: Voltage-gated Potassium (KV) ChannelsSummary: Kv1.3 blocker
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B7590 QuinidineTarget: Voltage-gated Sodium (NaV) Channels|Cytochrome P450 (CYP450)Summary: reduces both Na+ and K+ channel currents
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B7705 Lithium carbonateTarget: Na /K ATPasesSummary: Na+/K+ ATPase pump inhibitor
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B5351 SNX 482Target: Voltage-gated Calcium Channels (CaV)Summary: voltage-dependent R-type CaV2.3 calcium channel blocker
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B5515 ProTx IITarget: Voltage-gated Sodium (NaV) ChannelsSummary: NaV1.7 channel blocker