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.
- B7651 Tertiapin LQSummary: Kir1.1 channel blocker
- B7684 DigoxinSummary: Na+/K+ ATPase pump inhibitor
- B7705 Lithium carbonateTarget: Na /K ATPasesSummary: Na+/K+ ATPase pump inhibitor
- B7706 Gadolinium chlorideSummary: A calcium-sensing receptor (CaSR) agonist
- B7728 9-PhenanthrolSummary: TRPM4 blocker
- B7732 BCHSummary: L-type amino acid transporter LAT1 inhibitor
- B7733 CHCSummary: Monocarboxylic acid transport (MCT) inhibitor
- B7766 Congo RedSummary: VGlut inhibitor/dye for amyloidosis,amyloid in the cell walls of plants and fungi,outer membrane of Gram-negative bacteria
- B7767 Rose BengalSummary: VGlut and vesicular monoamine transporter (VMAT) inhibitor
- B7769 BDS ISummary: Kv3.4 potassium channel blocker, potent and reversible