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.
- B7722 MaxiPostSummary: Potassium channel modulator
- B7751 GSK 2193874Summary: TRPV4 antagonist, potent and selective
- B5084 DL-TBOASummary: inhibitor of excitatory amino acid transporters
- B5086 CGP 55845 hydrochlorideTarget: GABAB ReceptorsSummary: GABAB receptor antagonist
- B1389 Amiodarone HClSummary: Anti-arrhythmic drug
- B1375 Dehydroepiandrosterone (DHEA)Summary: Endogenous steroid hormone
- B2100 HC-030031Target: TRPASummary: TRPA1 channel blocker,potent and selective
- B1627 (-)-MK 801Target: NMDA ReceptorsSummary: NMDA antagonist,potent and selective
- B1189 SAR7334Summary: Potent TRPC6 inhibitor
- B1038 MDL-29951Summary: Glycine antagonist of NMDA receptor activation