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.
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B6225 L-Cysteinesulfinic acidSummary: NMDA and mGlu receptor agonist -
B6234 2-HydroxysaclofenSummary: GABAB receptor antagonist -
B6823 Cl-HIBOSummary: desensitising AMPA receptor agonist -
B7390 PhenamilSummary: TRPP3 channel inhibitor -
B7480 K 858Summary: mitotic kinesin Eg5 inhibitor -
B5802 ICA 121431Summary: human NaV1.3 and NaV1.1 channels inhibitor -
B5888 RetigabineSummary: An activator of voltage-gated potassium channel, used as an anticonvulsant agent -
B1989 NisoldipineTarget: Voltage-gated Calcium Channels (CaV)Summary: calcium channel blocker -
B6231 (±)-Nipecotic acidSummary: GABA uptake inhibitor -
B7153 POM 1Summary: A potent Ecto-NTPDase inhibitor
