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.
- B7392 AM 1172Summary: Inhibitor of anandamide uptake and FAAH,potent and selective
- B7424 PD 173212Summary: N-type voltage-gated calcium channel blocker
- B7428 MargatoxinSummary: KV1.3 channel blocker
- B7430 BretazenilSummary: GABAA benzodiazepine site partial agonist
- B7502 NS 1619Summary: Large-conductance Ca2+-activated potassium (BKCa, KCa1.1) channel activator
- B7512 NPEC-caged-(S)-AMPASummary: AMPA receptor agonist
- B7532 NAADP tetrasodium saltSummary: Ca2+ mobilizing agent
- B7582 ATPγS tetralithium saltSummary: P2 purinergic receptor agonist
- B7590 QuinidineTarget: Voltage-gated Sodium (NaV) Channels|Cytochrome P450 (CYP450)Summary: reduces both Na+ and K+ channel currents
- B7591 Bepridil hydrochlorideSummary: Calcium channel blocker