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.
- B6592 CharybdotoxinSummary: inhibitor of the big conductance Ca2+-activated K+ channel
- B6614 Thapsigargin1 CitationTarget: Ca2 -ATPasesSummary: sarco-endoplasmic reticulum Ca2+-ATPases inhibitor
- B6646 A23187, free acidSummary: Ca2+ ionophore
- 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