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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B7589 CIQSummary: NMDA receptor potentiator -
B7591 Bepridil hydrochlorideSummary: Calcium channel blocker -
B7722 MaxiPostSummary: Potassium channel modulator -
B7164 U 90042Summary: GABAA receptor ligand -
B7478 5,7-Dichlorokynurenic acid sodium saltSummary: NMDA receptor antagonist -
B7542 YM 58483Summary: A store-operated Ca2+ entry (SOCE) blocker -
B7711 ML 277Summary: Kv7.1 (KCNQ1) potassium channel activator -
B7151 17-PASummary: GABAA receptor antagonist -
B7473 DL-AP5 Sodium saltSummary: NMDA receptor antagonist -
B7659 Psora 41 CitationTarget: Voltage-gated Potassium (KV) ChannelsSummary: Kv1.3 blocker
