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.
- A3604 MibefradilTarget: Voltage-gated Calcium Channels (CaV)Summary: Calcium channel blocker
- A3605 Mibefradil dihydrochlorideSummary: Ca2+ channel blocker ,antihypertensive
- A3626 ML-7 hydrochlorideTarget: Myosin light chain kinases (MLCKs)Summary: Myosin light chain kinase inhibitor
- A3662 NNC 55-0396Target: Voltage-gated Calcium Channels (CaV)Summary: T-type calcium channel blocker
- A3663 NoopeptSummary: Nootropic and neuroprotective agent
- A3666 NP118809Summary: N-type calcium channel blocker
- A3668 NS309Summary: Calcium-Activated Potassium Channel activator
- A3699 PAP-1Summary: Kv1.3 inhibitor
- A3758 Retigabine dihydrochlorideSummary: Antiepileptic compound
- A3783 S0859Summary: NBC inhibitor,potent and selective