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.
- A3418 Flecainide acetateTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Antiarrhythmic drug
- B4798 Procainamide HClTarget: DNA MethyltransferasesSummary: sodium channel blocker
- B5895 CARIPORIDETarget: NHESummary: Potent NHE inhibitor
- B5515 ProTx IITarget: Voltage-gated Sodium (NaV) ChannelsSummary: NaV1.7 channel blocker
- B2249 Lamotrigine1 CitationTarget: 5-HT receptors|sodium channelSummary: 5-HT inhibitor, sodium channel blocker
- B2274 Proparacaine HClTarget: Voltage-gated Sodium (NaV) ChannelsSummary: voltage-gated sodium channels antagonist
- B2278 Ibutilide FumarateTarget: Voltage-gated Potassium (KV) Channels|Voltage-gated Calcium Channels (CaV)|sodium channelSummary: Class III antiarrhythmic agent
- B2272 Phenytoin sodiumTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Sodium channel stabilizer
- B1420 Bupivacaine HClTarget: Voltage-gated Sodium (NaV) ChannelsSummary: Anaesthetic drug
- A8513 RiluzoleTarget: Voltage-gated Sodium (NaV) Channels|glutamate releaseSummary: Sodium channel protein inhibitor