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.
- B5418 RuBi-GABASummary: Ruthenium-bipyridine-triphenylphosphine caged GABA
- B5419 GLYX 13Summary: NMDA receptor partial agonist
- B5453 RuBi-4APSummary: voltage-dependent K+ channel blocker
- B5460 EnterostatinSummary: Activator of the ERK and cAMP signaling pathways
- B5479 Pep2m, myristoylatedSummary: inhibitor of the interaction between AMPA receptor and N-ethylmaleimide-sensitive fusion protein (NSF)
- B5501 cis-Ned 19Summary: nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist
- B5515 ProTx IITarget: Voltage-gated Sodium (NaV) ChannelsSummary: NaV1.7 channel blocker
- B5523 TCN 237 dihydrochlorideSummary: NR2B-selective NMDA receptor antagonist
- B5533 Conantokin GSummary: NR2B-selective NMDA receptor antagonist
- B5676 ProTx ISummary: CaV3.1 channel blocker