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.
- B7260 NS 1643Summary: hERG KV11.1 channel activator
- B7268 DMCM hydrochlorideSummary: Benzodiazepine inverse agonist
- B7269 L-651,582Summary: Ca2+ channel blocker, orally active
- B7274 GYKI 47261 dihydrochlorideSummary: AMPA receptor antagonist, non-competitive and selective
- B7286 KM 11060Summary: Corrects F508del-CFTR trafficking
- B7311 PolygodialSummary: TRPA1 channel activator
- B7319 CGP 36216 hydrochlorideSummary: Selective GABAB antagonist
- B7331 L-838,417Summary: Subtype-selective GABAA receptor partial agonist
- B7332 KC 12291 hydrochlorideSummary: voltage-gated sodium channel blocker
- B7335 SB 452533Target: TRPVSummary: TRPV1 antagonist