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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C5110 FluspirileneSummary: potent, non-competitive antagonist of agonist-activated L-type calcium channels -
B7268 DMCM hydrochlorideSummary: Benzodiazepine inverse agonist -
C6823 2,2,2-Trichloroethanol -
C4851 MethsuximideSummary: anticonvulsant medication -
C5045 ML-297Summary: Selective Kir3.1/3.2 (GIRK1/2) channel activator -
B7254 Valerenic acidSummary: Positive allosteric modulator of GABAA receptor -
C3727 Barnidipine (hydrochloride)Summary: calcium-channel blocker -
C4778 VU590 (hydrochloride)Summary: inhibitor of KCNJ1 -
B7214 TB 21007Summary: GABAA receptor inverse agonist -
B7789 Huwentoxin XVISummary: N-type Ca2+ channel blocker,potent and selective
