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.
- B6976 STEARDASummary: potentiates TRPV1-mediated effects of NADA
- B6982 (±)-HIP-ASummary: excitatory amino acid transporter (EAAT) blocker
- B6983 (±)-HIP-BSummary: excitatory amino acid transporter (EAAT) blocker
- B6992 CGS 9343BSummary: Calmodulin antagonist
- B7015 QX 314 chlorideSummary: A voltage-activated Na+ channel blocker
- B7066 TNP-ATP triethylammonium saltSummary: P2X receptor antagonist
- B7082 NonactinSummary: Monovalent cation ionophore that displays selectivity for K+ and NH4+
- B7106 Calmidazolium chlorideSummary: Calmodulin antagonist
- B7153 POM 1Summary: A potent Ecto-NTPDase inhibitor
- B7161 ACETSummary: GluR5-containing kainate receptor antagonist