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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B7702 A 967079Summary: Selective TRPA1 channel blocker -
C3564 2,3-Butanedione-2-monoximeSummary: myosin ATPase inhibitor -
B6350 FG 7142Summary: benzodiazepine inverse agonist and anxiogenic agent -
B6591 IberiotoxinSummary: blocker of the big conductance Ca2+-activated K+ channel -
B5289 CALP2Summary: Cell-permeable calmodulin (CaM) antagonist -
B6247 5,7-Dichlorokynurenic acidSummary: NMDA receptor antagonist -
B7135 Co 102862Summary: voltage-gated sodium channel blocker -
B7225 CP 465022 hydrochlorideSummary: AMPA receptor antagonist, non-competitive and selective -
B7588 HC 067047Summary: TRPV4 antagonist -
B7182 Philanthotoxin 74Summary: AMPA receptor antagonist
