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.
- B6648 BHQSummary: inhibitor of endoplasmic reticulum Ca2+-ATPase
- B6665 D-CPP-eneSummary: NMDA antagonist
- B6668 (-)-Xestospongin CSummary: IP3-dependent Ca2+ release inhibitor
- B6670 ARL 67156 trisodium saltSummary: ecto-ATPase inhibitor
- B6675 Ochratoxin ASummary: endoplasmic reticulum ATP-dependent calcium pump activator
- B6683 UCL 1684Summary: apamin-sensitive Ca2+-activated K+ channel (KCa2.1) blocker
- B6704 5'-IodoresiniferatoxinSummary: TRPV1 (VR1) receptor antagonist
- B6740 Ruthenium RedSummary: Blocks Ca2+ uptake and release, and voltage-sensitive Ca2+ channels
- B6750 PPAHVSummary: vanilloid TRPV1 (VR1) receptor agonist
- B6752 Suramin hexasodium saltSummary: DNA topoisomerase II inhibitor