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.
- C3709 EniporideSummary: Na+/H+ exchange inhibitor
- C3840 Estradiol 17-(β-D-Glucuronide) (sodium salt)Summary: substrate of the multidrug resistance protein 2 (MRP2)
- C4082 Eicosapentaenoyl SerotoninSummary: TRPV1 channel inhibitor
- C4167 Oleoyl SerotoninSummary: TRPV1 channel inhibitor
- C4169 Palmitoyl SerotoninSummary: TRPV1 channel inhibitor
- C4170 Stearoyl SerotoninSummary: TRPV1 channel inhibitor
- C4171 Docosahexaenoyl SerotoninSummary: TRPV1 channel inhibitor
- C4398 CP-465022 (maleate)Summary: AMPA antagonist
- C4375 Bafilomycin DSummary: vacuolar H+ ATPases (V-ATPases) inhibitor
- C4546 VerruculogenSummary: Maxi-K potassium channels inhibitor