Membrane Transporter/Ion Channel


Membrane Transporters mediate the movement of ions and molecules via binding and moving the substance across the membrane. There are two main actions of transporter: facilitated diffusion (passive transport) and active transport. Membrane transporters which bind the hydrolysis of ATP to the transport of target molecules are referred to as ATPases. For instance, Na+,K+-ATPases or Na+,K+-pumps are responsible for the transport of Na+ out of and K+ into cells.
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.
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N2951 Lanatoside CSummary: Lanatoside C is a cardiac glycoside and Na⁺/K⁺⁺-ATPase modulator used to investigate ion-transport signaling and cell physiology in pharmacological research. -
BA6578 FlunarizineSummary: An orally active dual Na+/Ca2+ channel blocker with D2 dopamine receptor antagonistic activity. -
BA6579 TrimethadioneSummary: A T-type calcium channel blocker. -
BA6587 NicardipineSummary: A dihydropyridine cardiac calcium channel blocker. -
BA6742 MephenesinSummary: An NMDA receptor antagonist and centrally acting muscle relaxant. -
BA6771 OrphenadrineSummary: A non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist. -
BA6920 N-AcetylprocainamideSummary: A potassium channel blocker that modulates action potential duration. -
BA6991 MepivacaineSummary: An amide-type voltage-gated sodium channel inhibitor. -
C9052 NedisertibSummary: A small-molecule DNA-PKcs inhibitor for scientific research on DNA double-strand break repair. -
C9055 V-9302Summary: A selective small-molecule tool compound that inhibits ASCT2, used for in vitro analysis of glutamine transport.
