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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B5554 A 784168Summary: TRPV1 antagonist,potent and selective -
B5566 CMPDASummary: positive allosteric modulator of AMPA receptors -
B5570 TC-P 262Summary: P2X3 and P2X2/3 receptor antagonist -
B5572 Ro 51Summary: dual P2X3 and P2X2/3 antagonist -
B5582 OcinaplonSummary: GABAA receptors modulator -
B5584 TP 003Summary: GABAA receptor (α3 subtype) partial agonist -
B5585 MK 0343Summary: GABAA partial agonist -
B5594 TC-N 1752Summary: human NaV1.7 channels blocker -
B5605 NS 3623Summary: human ether-a-go-go (hERG) KV11.1 potassium channel activator -
B5613 A 804598Summary: P2X7 antagonist,potent and selective

