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.
- B5793 GMQ hydrochlorideSummary: acid-sensing ion channel 3 (ASIC3) opener
- B5802 ICA 121431Summary: human NaV1.3 and NaV1.1 channels inhibitor
- B5805 LDN 212320Summary: increases expression of glutamate transporter EAAT2
- B6208 Dihydrokainic acidSummary: EAAT2(GLT1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake
- B6221 L-Quisqualic acidSummary: AMPA receptors and metabotropic glutamate receptors agonist
- B6226 Kainic acidSummary: kainate receptor agonist, selective
- B6238 (S)-AMPASummary: AMPA agonist
- B6566 NBQX disodium saltSummary: A potent, highly selective and competitive AMPA receptor antagonist
- B6567 CNQX disodium saltSummary: AMPA/kainate antagonist
- B6585 (RS)-AMPA hydrobromideSummary: AMPAR agonist