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.
-   B7142 L-364,373Summary: KV7.1 (KCNQ1) channel activator B7142 L-364,373Summary: KV7.1 (KCNQ1) channel activator
-   B6668 (-)-Xestospongin CSummary: IP3-dependent Ca2+ release inhibitor B6668 (-)-Xestospongin CSummary: IP3-dependent Ca2+ release inhibitor
-   B6658 SDZ 220-040Summary: NMDA receptor antagonist B6658 SDZ 220-040Summary: NMDA receptor antagonist
-   B6771 CGP 7930Summary: Positive allosteric modulator of GABAB receptors B6771 CGP 7930Summary: Positive allosteric modulator of GABAB receptors
-   B7093 DPO-1Summary: Blocker of IKur ultrarapid delayed rectifier potassium current and KV1.5 channels B7093 DPO-1Summary: Blocker of IKur ultrarapid delayed rectifier potassium current and KV1.5 channels
-   B6646 A23187, free acidSummary: Ca2+ ionophore B6646 A23187, free acidSummary: Ca2+ ionophore
-   B7082 NonactinSummary: Monovalent cation ionophore that displays selectivity for K+ and NH4+ B7082 NonactinSummary: Monovalent cation ionophore that displays selectivity for K+ and NH4+
-   B6652 CGS 19755Summary: NMDA receptor antagonist B6652 CGS 19755Summary: NMDA receptor antagonist
-   B6692 L-655,708Summary: inverse agonist for the benzodiazepine site of GABAA receptors containing the α5 subunit B6692 L-655,708Summary: inverse agonist for the benzodiazepine site of GABAA receptors containing the α5 subunit
-   B6643 2-APBSummary: antagonist of Ins(1,4,5) P3-induced Ca2+ release B6643 2-APBSummary: antagonist of Ins(1,4,5) P3-induced Ca2+ release
