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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B6077 E-4031Summary: antiarrhythmic agent blocking the ATP-sensitive potassium channel -
B3483 LercanidipineSummary: calcium channel blocker -
B6228 Quinolinic acidSummary: NMDA agonist -
B7684 DigoxinSummary: Na+/K+ ATPase pump inhibitor -
B6235 SaclofenSummary: GABAB receptor antagonist -
B6849 UBP 282Summary: AMPA and kainate receptor antagonist -
B7492 RN 1747Summary: TRPV4 agonist -
B5850 GS967Summary: inhibitor of cardiac late sodium current -
C5579 Brilliant Blue GSummary: used for protein staining in SDS-PAGE, Blue Native PAGE, and the Bradford Method; selective inhibitor of the P2X purinoceptor channel P2X7 -
B3482 Lercanidipine hydrochlorideSummary: calcium channel blocker
