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.
- B7180 Naspm trihydrochlorideSummary: A Ca2+-permeable AMPA receptor antagonist
- B7192 ω-Agatoxin IVASummary: P-type calcium channels blocker
- B7193 ω-Agatoxin TKSummary: CaV2.1 P/Q-type calcium channels blocker
- B7211 Fumitremorgin CSummary: multidrug transporter inhibitor
- B7220 NBMPRSummary: Equilibrative nucleoside transporter 1 (ENT1) inhibitor
- B7239 SarcosineSummary: Endogenous inhibitor of GlyT1
- B7254 Valerenic acidSummary: Positive allosteric modulator of GABAA receptor
- B7256 RO-3Summary: homomeric P2X3 and heteromeric P2X2/3 receptor antagonist
- B7262 Tetraethylammonium chlorideSummary: K+ channel blocker
- B7358 BzATP (ammonium salt)1 CitationSummary: A P2X7 receptor agonist