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.
- B5258 CALP1Summary: Cell-permeable calmodulin (CaM) agonist
- B5271 PDZ1 Domain inhibitor peptideSummary: Novel cyclic peptide that disrupts interaction between GluR6 and PSD-95
- B5276 MNI-caged-NMDASummary: NMDA caged with the photosensitive 4-methoxy-7-nitroindolinyl group
- B5289 CALP2Summary: Cell-permeable calmodulin (CaM) antagonist
- B5291 CALP3Summary: Cell-permeable calmodulin (CaM) agonist
- B5343 HU 211Summary: NMDA antagonist, novel and non-competitive
- B5351 SNX 482Target: Voltage-gated Calcium Channels (CaV)Summary: voltage-dependent R-type CaV2.3 calcium channel blocker
- B5378 Conantokin-TSummary: Non-competitive NMDA receptor antagonist
- B5393 ShK-Dap22Summary: Extremely potent KV1.3 channel blocker
- B5409 ZD 9379Summary: NMDA receptor antagonist