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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B7106 Calmidazolium chlorideSummary: Calmodulin antagonist -
B6915 Ro 15-4513Summary: benzodiazepine ligand -
B6998 PPPASummary: NMDA receptor antagonist -
B6992 CGS 9343BSummary: Calmodulin antagonist -
B7502 NS 1619Summary: Large-conductance Ca2+-activated potassium (BKCa, KCa1.1) channel activator -
B6914 ZK 93426 hydrochlorideSummary: benzodiazepine receptor antagonist,competitive -
B6997 PMPA (NMDA antagonist)Summary: Competitive NMDA receptor antagonist -
B7500 BL 1249Summary: K2P2.1 (TREK-1) channel opener -
B6947 Ionomycin free acidTarget: Calcium ionophoresSummary: calcium ionophore -
B6880 MRS 1845Summary: store-operated Ca2+ channels blocker
