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.
- B1290 Lansoprazole sodiumSummary: PPI/cytochrome P450 inhibitor
- C3007 Oligomycin ComplexSummary: inhibits mitochondrial membrane-bound ATP synthases
- C3286 ClopamideSummary: sodium/chloride cotransporters inhibitor
- C4125 Ethacrynic AcidSummary: A loop diuretic that inhibits the Na+/K+/2Cl- cotransporter (NKCC2)
- C6540 Ethosuximide
- C6622 6-Methylflavone
- B5177 OMDM-2Summary: Metabolically stable inhibitor of anandamide cellular uptake
- B5245 6-IodonordihydrocapsaicinSummary: Vanilloid receptor antagonist
- B5286 MNI-caged-D-aspartateSummary: Agonist at NMDA receptors and EAAT substrate
- B5288 DNQX disodium saltSummary: Selective non-NMDA receptor antagonist