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.
-   B6411 L-701,252Summary: glycine-NMDA site antagonist B6411 L-701,252Summary: glycine-NMDA site antagonist
-   B6562 TPMPASummary: GABAA-ρ antagonist B6562 TPMPASummary: GABAA-ρ antagonist
-   B6721 CP 339818 hydrochlorideSummary: KV1.3 channel antagonist B6721 CP 339818 hydrochlorideSummary: KV1.3 channel antagonist
-   B7626 A 887826Summary: voltage-dependent Nav1.8 sodium channel blocker B7626 A 887826Summary: voltage-dependent Nav1.8 sodium channel blocker
-   C4398 CP-465022 (maleate)Summary: AMPA antagonist C4398 CP-465022 (maleate)Summary: AMPA antagonist
-   B5676 ProTx ISummary: CaV3.1 channel blocker B5676 ProTx ISummary: CaV3.1 channel blocker
-   C7128 TRPM8 antagonist WS-3 C7128 TRPM8 antagonist WS-3
-   B6386 Synthalin sulfateSummary: NMDA receptor antagonist B6386 Synthalin sulfateSummary: NMDA receptor antagonist
-   B6487 Chlormethiazole hydrochlorideSummary: GABAA agonist B6487 Chlormethiazole hydrochlorideSummary: GABAA agonist
-   B6712 LevcromakalimSummary: prototypical Kir6 (KATP) channel opener B6712 LevcromakalimSummary: prototypical Kir6 (KATP) channel opener
