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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N2617 Ginsenoside RcSummary: Anticancer, antidiabetic and neuroprotective agent -
N2202 Loureirin B1 CitationSummary: a member of dihydrochalcones -
N2418 Linalool -
A8208 Tariquidar2 CitationTarget: P-glycoprotein (P-gp)Summary: P-glycoprotein inhibitor,potent and non-competitive -
A2700 10Panx1 CitationTarget: Gap JunctionsSummary: Panx-1 mimetic inhibitor -
A2701 Scrambled 10PanxSummary: Panx-1 mimetic inhibitory peptide, blocks pannexin-1 gap junctions -
A3100 (+)-MK 801Target: NMDA ReceptorsSummary: Potent NMDA antagonist -
A3130 A 438079Summary: P2X7 receptor antagonist,competitive and selective -
A3131 A 438079 hydrochlorideSummary: P2X7 receptor antagonist,competitive and selective -
A3134 A-317491Summary: P2X3 and P2X2/3 receptor antagonist

