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Membrane Transporter/Ion Channel

Membrane Transporters mediate the movement of ions and molecules via binding and moving the substance across the membrane. There are two main actions of transporter: facilitated diffusion (passive transport) and active transport. Membrane transporters which bind the hydrolysis of ATP to the transport of target molecules are referred to as ATPases. For instance, Na+,K+-ATPases or Na+,K+-pumps are responsible for the transport of Na+ out of and K+ into cells.

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.

Items 901-910 of 925

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  1. Elexacaftor (VX-445)
    C8980 Elexacaftor (VX-445)
    Summary: Elexacaftor (VX-445; CAS 2216712-66-0) is a CFTR corrector modulating F508del-CFTR processing and trafficking, widely utilized in cystic fibrosis mechanism and ion-channel biology research.
  2. Fosphenytoin (disodium)
    C9020 Fosphenytoin (disodium)
    Summary: Fosphenytoin (disodium) is a water-soluble phenytoin prodrug modulating voltage-gated sodium channels, widely utilized in neuropharmacology and neuronal excitability research.
  3. Glafenine HCl
    C9022 Glafenine HCl
    Summary: Glafenine HCl is a fenamate-derived nonsteroidal anti-inflammatory compound used as a pharmacological tool in cyclooxygenase signaling and inflammation-related biochemical research.
  4. Brucine sulfate heptahydrate
    C9033 Brucine sulfate heptahydrate
    Summary: Brucine sulfate heptahydrate is a strychnos alkaloid and glycine receptor antagonist used as a biochemical probe in neuropharmacology and receptor signaling research.
  5. Bulleyaconi cine A
    N2908 Bulleyaconi cine A
    Summary: Bulleyaconi cine A is a diterpenoid alkaloid investigated for modulation of voltage-gated sodium channels in neuropharmacology and pain-signaling mechanism research.
      ≥16.67 mg/mL
  6. Securinine
    N2910 Securinine
    Summary: Securinine is a plant-derived GABA_A receptor antagonist modulating inhibitory neurotransmission, widely utilized as a pharmacological probe in neuropharmacology and synaptic signaling research.
  7. Crocetin
    BA8418 Crocetin
    Summary: Crocetin (Transcrocetin) is extracted from saffron.
  8. Phellopterin
    BA8685 Phellopterin
    Summary: An orally active furocoumarin that acts as a partial agonist of central benzodiazepine receptors, with anti-inflammatory activity via SIRT1 upregulation
      ≥39.2 mg/mL
  9. Elobixibat
    BA3536 Elobixibat
    Summary: Elobixibat (A3309; AZD7806) is an orally effective inhibitor with values of 0.53 nM (human IBAT), 0.13 nM (mouse IBAT), and 5.8 nM (canine IBAT), respectively.
  10. 1,4-Cineole
    N2917 1,4-Cineole
    Summary: 1,4-Cineole is a monoterpene oxide investigated for modulating inflammatory and oxidative stress signaling pathways in pharmacology, toxicology, and cellular mechanism research.

Items 901-910 of 925

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