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.
-
B7532 NAADP tetrasodium saltSummary: Ca2+ mobilizing agent -
B7081 (-)-Bicuculline methiodideSummary: GABAA receptor antagonist -
B7372 Ro 8-4304 hydrochlorideSummary: NMDA receptor antagonist -
B7424 PD 173212Summary: N-type voltage-gated calcium channel blocker -
B7651 Tertiapin LQSummary: Kir1.1 channel blocker -
B7068 CGS 20625Summary: partial agonist for the benzodiazepine binding site of the GABAA receptor -
B7212 threo Ifenprodil hemitartrateSummary: σ receptor agonist and NR2B subunit-selective NMDA receptor antagonist -
B7269 L-651,582Summary: Ca2+ channel blocker, orally active -
B7643 GW 542573XSummary: Activator of small-conductance Ca2+-activated K+ channels (KCa2) -
B7186 TCS 46bSummary: NR1A/NR2B NMDA receptor antagonist,orally active
