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  2. List of investigational analgesics - Wikipedia

    en.wikipedia.org/wiki/List_of_investigational...

    This is a list of investigational analgesics, or analgesics that are currently under development for clinical use but are not yet approved. Chemical/generic names are listed first, with developmental code names, synonyms, and brand names in parentheses. This list was last comprehensively updated in June 2017. It is likely to become outdated ...

  3. Persistent sodium current - Wikipedia

    en.wikipedia.org/wiki/Persistent_Sodium_Current

    Pharmacological blockers of INaP are used clinically in many of these disorders. Amiodarone, while primarily blocking the human Ether-a-go-go-Related Gene potassium channel, has shown to significantly reduce persistent sodium current by 50% in cortical neurons [14] as well as in cardiac sodium channel NaV1.5 and is used to treat arrhythmia. [15]

  4. Suzetrigine - Wikipedia

    en.wikipedia.org/wiki/Suzetrigine

    Suzetrigine (developmental code name VX-548) is a non-opioid, small-molecule analgesic that works as a selective inhibitor of Na v 1.8-dependent pain-signaling pathways in the peripheral nervous system. [1] [2] It is being developed by Vertex Pharmaceuticals and has completed two phase 3 clinical trials. [1] [3]

  5. Sodium channel blocker - Wikipedia

    en.wikipedia.org/wiki/Sodium_channel_blocker

    Sodium channel blockers are also used as local anesthetics and anticonvulsants. [5] Sodium channel blockers have been proposed for use in the treatment of cystic fibrosis, [6] but current evidence is mixed. [7] It has been suggested that the analgesic effects of some antidepressants may be mediated in part via sodium channel blockade. [8]

  6. Channel modulator - Wikipedia

    en.wikipedia.org/wiki/Channel_modulator

    Potassium channel: see also Potassium channel blocker, Potassium channel opener; Sodium channel: see also Sodium channel blocker, Sodium channel opener; Chloride channel: see also Chloride channel blocker, Chloride channel opener; Transient receptor potential channel; Ligand gated ion channels. 5-HT3: see also 5-HT3 antagonist,

  7. Channel blocker - Wikipedia

    en.wikipedia.org/wiki/Channel_blocker

    Sodium channel inhibitors are used as both antiepileptics and antiarrhythmics, as they can inhibit the hyper-excitable tissues in a patient. [22] Introducing specific sodium channel blockers into a tissue allows for the preferential binding of the blocker to sodium channels, which results in an ultimate inhibition of the flow of sodium into the ...

  8. Channel opener - Wikipedia

    en.wikipedia.org/wiki/Channel_opener

    A channel opener, also known as a channel activator, is a type of drug which facilitates ion flow through ion channels. They include the following: Potassium channel openers; Calcium channel openers; Sodium channel openers; Chloride channel openers

  9. Category:Sodium channels - Wikipedia

    en.wikipedia.org/wiki/Category:Sodium_channels

    Sodium channel blockers (1 C, 77 P) Sodium channel openers (1 C, 11 P) Pages in category "Sodium channels" ... Code of Conduct;