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.
- B6816 8-CPT-2Me-cAMP, sodium saltTarget: EpacSummary: EPAC activator, selective
- B6817 ApaminSummary: small-conductance Ca2+-activated K+-channel (KCa2, SK) inhibitor
- B6831 Autocamtide-2-related inhibitory peptideTarget: Ca2 /calmodulin-dependent protein kinases (CaMKs)Summary: inhibitor of calmodulin-dependent protein kinase II (CaM-kinase II, CaMKII)
- B6846 ALX 5407 hydrochlorideSummary: GlyT1 inhibitor,selective non-transportable
- B6861 SR 33805 oxalateSummary: Ca2+ channel antagonist
- B6920 PaxillineSummary: high-conductance Ca2+-activated K+ (BKCa, KCa1.1) channels blocker
- B6947 Ionomycin free acidTarget: Calcium ionophoresSummary: calcium ionophore
- B6953 SCSSummary: GABAA receptor antagonist
- B6959 HispidulinSummary: Partial positive allosteric modulator at the benzodiazepine receptor
- B6975 PALDASummary: potentiates TRPV1-mediated effects of NADA