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.
- B7349 AP 18Summary: Reversible TRPA1 channel blocker
- B7359 rac BHFFSummary: GABAB receptor positive allosteric modulator
- B7362 AZ 11645373Summary: Human P2X7 antagonist,potent and selective
- B7372 Ro 8-4304 hydrochlorideSummary: NMDA receptor antagonist
- B7385 JNJ 17203212Summary: TRPV1 antagonist
- B7388 ValinomycinTarget: IonophoresSummary: potassium-specific transporter
- B7389 EIPA3 CitationTarget: Na /H Exchangers (NHEs)Summary: TRPP3 channel inhibitor
- B7390 PhenamilSummary: TRPP3 channel inhibitor
- B7391 BenzamilSummary: Na+/Ca2+ exhanger (NCX) inhibitor
- B7394 LY 2365109 hydrochlorideSummary: glycine transporter 1 (GlyT1) inhibitor