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Funapide

From Wikipedia, the free encyclopedia
Analgesic drug under development
Pharmaceutical compound
Funapide
Clinical data
Routes of
administration
By mouth,topical
ATC code
  • None
Identifiers
  • (7S)-1'-[[5-(trifluoromethyl)furan-2-yl]methyl]spiro[6H-furo[2,3-f][1,3]benzodioxole-7,3'-indole]-2'-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
Chemical and physical data
FormulaC22H14F3NO5
Molar mass429.351 g·mol−1
3D model (JSmol)
  • C1C2(C3=CC=CC=C3N(C2=O)CC4=CC=C(O4)C(F)(F)F)C5=CC6=C(C=C5O1)OCO6
  • InChI=1S/C22H14F3NO5/c23-22(24,25)19-6-5-12(31-19)9-26-15-4-2-1-3-13(15)21(20(26)27)10-28-16-8-18-17(7-14(16)21)29-11-30-18/h1-8H,9-11H2/t21-/m0/s1
  • Key:NEBUOXBYNAHKFV-NRFANRHFSA-N

Funapide (INN; former developmental codesTV-45070 andXEN402) is a novelanalgesic under development byXenon Pharmaceuticals (formerly in partnership withTeva Pharmaceutical Industries) for the treatment of a variety ofchronic pain conditions, includingosteoarthritis,neuropathic pain,postherpetic neuralgia, anderythromelalgia, as well asdental pain.[1][2][3][4] It acts as asmall-moleculeNav1.7 andNav1.8voltage-gated sodium channelblocker.[1][2][4] Funapide was evaluated in humans in bothoral andtopical formulations, and as of July 2014, had reachedphase IIbclinical trials.[1][3]Development of the drug was discontinued in 2022.[5]

See also

[edit]

References

[edit]
  1. ^abcBagal SK, Chapman ML, Marron BE, Prime R, Storer RI, Swain NA (August 2014)."Recent progress in sodium channel modulators for pain".Bioorganic & Medicinal Chemistry Letters.24 (16):3690–3699.doi:10.1016/j.bmcl.2014.06.038.PMID 25060923.
  2. ^abAli Z, Palmer JE,Goli V (2013). "Anticonvulsants: Clinical". In McMahon S, Koltzenburg M, Tracey I, Turk DC (eds.).Wall & Melzack's Textbook of Pain (6 ed.). Elsevier Health Sciences. p. 508.ISBN 978-0-7020-4059-7.OCLC 1008841684.
  3. ^ab"TV-45070: A Small Molecule for the Treatment of the Orphan Disease EM and Other Pain Disorders".Xenon Pharma. Archived fromthe original on 15 July 2013.
  4. ^ab"Teva and Xenon Announce Teva's World Wide License of Xenon's Pain Drug XEN402".Xenon Pharma. 11 December 2012. Archived fromthe original on 26 July 2014. Retrieved2014-07-20.
  5. ^"Funapide - Flexion Therapeutics".AdisInsight. Springer Nature Switzerland AG.
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Acetates
COX-2 inhibitors
Fenamates
Salicylates
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Cannabinoids
Ion channel
modulators
Calcium blockers
Sodium blockers
Potassium openers
Myorelaxants
Others
Esters by acid
Aminobenzoic
Benzoic
ArCO2- (not para-amino or Ph)
Amides
Combinations
Calcium
VDCCsTooltip Voltage-dependent calcium channels
Blockers
Activators
Potassium
VGKCsTooltip Voltage-gated potassium channels
Blockers
Activators
IRKsTooltip Inwardly rectifying potassium channel
Blockers
Activators
KCaTooltip Calcium-activated potassium channel
Blockers
Activators
K2PsTooltip Tandem pore domain potassium channel
Blockers
Activators
Sodium
VGSCsTooltip Voltage-gated sodium channels
Blockers
Activators
ENaCTooltip Epithelial sodium channel
Blockers
Activators
ASICsTooltip Acid-sensing ion channel
Blockers
Chloride
CaCCsTooltip Calcium-activated chloride channel
Blockers
Activators
CFTRTooltip Cystic fibrosis transmembrane conductance regulator
Blockers
Activators
Unsorted
Blockers
Others
TRPsTooltip Transient receptor potential channels
LGICsTooltip Ligand gated ion channels


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