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.
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B2277 A-803467Target: Voltage-gated Sodium (NaV) ChannelsSummary: NaV1.8 channel blocker,potent and selective
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A2917 FlumazenilTarget: GABAA ReceptorsSummary: Benzodiazepine antagonist
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A1958 EtomidateTarget: GABAA ReceptorsSummary: General anesthetic with GABA modulatory and GABA-mimetic actions
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A1888 TRAM-34Target: Calcium-Activated Potassium (KCa) ChannelsSummary: KCa3.1 blocker,potent and highly selective
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A1855 BumetanideTarget: Na /K /Cl- Symporters (NKCCs)Summary: NKCC cotransporter inhibitor
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A5354 ZonisamideTarget: Voltage-gated Sodium (NaV) Channels|Voltage-gated Calcium Channels (CaV)|Carbonic Anhydrases|Calcium-Activated Potassium (KCa) ChannelsSummary: Antiepileptic with anticonvulsant and mechanistic effect
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A1174 AMG-517Target: TRP ChannelSummary: TRPV1 antagonist,potent and highly selective
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A8349 Omecamtiv mecarbilTarget: MyosinSummary: Cardiac myosin activator
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B5895 CARIPORIDETarget: NHESummary: Potent NHE inhibitor
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B5410 AZ 10606120 dihydrochlorideTarget: P2X ReceptorsSummary: Potent P2X7 receptor antagonist