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.
- C4851 MethsuximideSummary: anticonvulsant medication
- C5045 ML-297Summary: Selective Kir3.1/3.2 (GIRK1/2) channel activator
- C5049 AZD 3965Summary: potent inhibitor of monocarboxylate transporter 1 (MCT1)
- C5110 FluspirileneSummary: potent, non-competitive antagonist of agonist-activated L-type calcium channels
- C5039 Quinacrine (hydrochloride hydrate)Summary: voltage-dependent sodium channels blocker
- C5065 GSK1016790ASummary: TRPV4 agonist
- C5294 Guanidinoethyl sulfonateSummary: competitive glycine receptor antagonist
- C5579 Brilliant Blue GSummary: used for protein staining in SDS-PAGE, Blue Native PAGE, and the Bradford Method; selective inhibitor of the P2X purinoceptor channel P2X7
- B1389 Amiodarone HClSummary: Anti-arrhythmic drug
- B1375 Dehydroepiandrosterone (DHEA)Summary: Endogenous steroid hormone