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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C4563 CapsiconiateSummary: TRPV1 agonist -
C4593 WZB117Summary: glucose transporter 1 (Glut1) inhibitor -
C4729 Bafilomycin C1Summary: vacuolar H+-ATPases (V-ATPases) inhibitor -
C4778 VU590 (hydrochloride)Summary: inhibitor of KCNJ1 -
C5010 IAA-94Summary: indanyloxyacetic acid (IAA) inhibitor -
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

