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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B7640 ICA 069673Summary: KV7.2/KV7.3 (KCNQ2/3) channel opener -
B6959 HispidulinSummary: Partial positive allosteric modulator at the benzodiazepine receptor -
B7193 ω-Agatoxin TKSummary: CaV2.1 P/Q-type calcium channels blocker -
B7062 Co 101244 hydrochlorideSummary: NR2B-containing NMDA receptor antagonist -
B7600 NS 5806Summary: KV4.3 channel activator -
B6953 SCSSummary: GABAA receptor antagonist -
B7192 ω-Agatoxin IVASummary: P-type calcium channels blocker -
B6918 GS 39783Summary: Positive allosteric modulator of GABAB receptor -
B7029 GavestinelSummary: NMDA receptor antagonist -
B7507 UK 78282 hydrochlorideSummary: KV1.3 and KV1.4 voltage-gated potassium channel blocker
