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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B6257 (R)-4-CarboxyphenylglycineSummary: NMDA receptor antagonist -
B6401 PK 111951 CitationTarget: benzodiazepine receptorSummary: An antagonist of the peripheral benzodiazepine receptor -
B6700 P1075Summary: Kir6 (KATP) channel opener -
B7517 LicarbazepineSummary: voltage-gated sodium channel blocker -
B7751 GSK 2193874Summary: TRPV4 antagonist, potent and selective -
C4729 Bafilomycin C1Summary: vacuolar H+-ATPases (V-ATPases) inhibitor -
B6683 UCL 1684Summary: apamin-sensitive Ca2+-activated K+ channel (KCa2.1) blocker -
B7728 9-PhenanthrolSummary: TRPM4 blocker -
B5351 SNX 482Target: Voltage-gated Calcium Channels (CaV)Summary: voltage-dependent R-type CaV2.3 calcium channel blocker -
B6254 (RS)-(Tetrazol-5-yl)glycineSummary: NMDA receptor agonist
