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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B6395 FGIN-1-43Summary: ligand as probe for the mitochondial DBI receptor (peripheral benzodiazepine receptor) -
B7274 GYKI 47261 dihydrochlorideSummary: AMPA receptor antagonist, non-competitive and selective -
B7332 KC 12291 hydrochlorideSummary: voltage-gated sodium channel blocker -
C4375 Bafilomycin DSummary: vacuolar H+ ATPases (V-ATPases) inhibitor -
B6249 N-(4-Hydroxyphenylacetyl)spermineSummary: NMDA receptor antagonist -
B6592 CharybdotoxinSummary: inhibitor of the big conductance Ca2+-activated K+ channel -
B5291 CALP3Summary: Cell-permeable calmodulin (CaM) agonist -
B6394 FGIN-1-27Summary: high affinity agonist of the translocator protein (TSPO,peripheral benzodiazepine receptor) -
B7219 VeratridineSummary: Voltage-gated Na+ channel opener -
B7240 CX 546Summary: AMPA receptor potentiator
