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.
- B2201 Zinc PyrithioneTarget: Proton PumpSummary: Proton pump inhibitor
- B2278 Ibutilide FumarateTarget: Voltage-gated Potassium (KV) Channels|Voltage-gated Calcium Channels (CaV)|sodium channelSummary: Class III antiarrhythmic agent
- B1530 Niflumic acidSummary: Ca2+-activated Cl- channel blocker
- B2272 Phenytoin sodiumTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Sodium channel stabilizer
- B2271 PhenytoinSummary: inactive voltage-gated sodium channel stabilizer
- B2195 GliclazideTarget: Inward Rectifier Potassium (Kir) ChannelsSummary: Potassium channel inhibitor
- B1413 Tetracaine HClSummary: Anaesthetic and allosteric inhibitor
- B1393 NitrendipineTarget: Voltage-gated Calcium Channels (CaV)Summary: Calcium channel blocker
- B1420 Bupivacaine HClTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Anaesthetic drug
- B2198 NateglinideTarget: Inward Rectifier Potassium (Kir) ChannelsSummary: Insulin secretagog agent