Jump to content
Wikipedia The Free Encyclopedia

Vixotrigine

From Wikipedia, the free encyclopedia
Analgesic drug under development
Pharmaceutical compound
Vixotrigine
Clinical data
Other namesRaxatrigine; CNV1014802; GSK-1014802; BIIB 074
Routes of
administration
By mouth
ATC code
  • None
Identifiers
  • (2S,5R)-5-[4-[(2-fluorophenyl)methoxy]phenyl]pyrrolidine-2-carboxamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
Chemical and physical data
Formula C18H19FN2O2
Molar mass 314.360 g·mol−1
3D model (JSmol)
  • C1CC(NC1C2=CC=C(C=C2)OCC3=CC=CC=C3F)C(=O)N
  • InChI=1S/C18H19FN2O2/c19-15-4-2-1-3-13(15)11-23-14-7-5-12(6-8-14)16-9-10-17(21-16)18(20)22/h1-8,16-17,21H,9-11H2,(H2,20,22)/t16-,17+/m1/s1
  • Key:JESCETIFNOFKEU-SJORKVTESA-N

Vixotrigine (INN Tooltip International Nonproprietary Name, USAN Tooltip United States Adopted Name), formerly known as raxatrigine (INN Tooltip International Nonproprietary Name, USAN Tooltip United States Adopted Name), is an analgesic which is under development by Convergence Pharmaceuticals for the treatment of lumbosacral radiculopathy (sciatica) and trigeminal neuralgia (TGN).[1] [2] [3] Vixotrigine was originally claimed to be a selective central Nav1.3 blocker, but was subsequently redefined as a selective peripheral Nav1.7 blocker.[citation needed ] Following this, vixotrigine was redefined once again, as a non-selective voltage-gated sodium channel blocker.[citation needed ] As of January 2018, it is in phase III clinical trials for trigeminal neuralgia and is in phase II clinical studies for erythromelalgia and neuropathic pain.[4] It was previously under investigation for the treatment of bipolar disorder, but development for this indication was discontinued.[4]

See also

[edit ]

References

[edit ]
  1. ^ "CNV1014802". Convergence Pharmaceuticals.
  2. ^ McMahon S, Koltzenburg M, Tracey I, Turk DC (1 March 2013). Wall & Melzack's Textbook of Pain: Expert Consult - Online. Elsevier Health Sciences. p. 508. ISBN 978-0-7020-5374-0.
  3. ^ Bagal 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年06月03日8 . PMID 25060923.
  4. ^ a b "Vixotrigine - Biogen". Adis Insight. Springer Nature Switzerland AG.
[edit ]
Opioids
Opiates/opium
Semisynthetic
Synthetic
Paracetamol-type
NSAIDs
Propionates
Oxicams
Acetates
COX-2 inhibitors
Fenamates
Salicylates
Pyrazolones
Others
Cannabinoids
Ion channel
modulators
Calcium blockers
Sodium blockers
Potassium openers
Myorelaxants
Others
Calcium
VDCCs Tooltip Voltage-dependent calcium channels
Blockers
Activators
Potassium
VGKCs Tooltip Voltage-gated potassium channels
Blockers
Activators
IRKs Tooltip Inwardly rectifying potassium channel
Blockers
Activators
KCa Tooltip Calcium-activated potassium channel
Blockers
Activators
K2Ps Tooltip Tandem pore domain potassium channel
Blockers
Activators
Sodium
VGSCs Tooltip Voltage-gated sodium channels
Blockers
Activators
ENaC Tooltip Epithelial sodium channel
Blockers
Activators
ASICs Tooltip Acid-sensing ion channel
Blockers
Chloride
CaCCs Tooltip Calcium-activated chloride channel
Blockers
Activators
CFTR Tooltip Cystic fibrosis transmembrane conductance regulator
Blockers
Activators
Unsorted
Blockers
Others
TRPs Tooltip Transient receptor potential channels
LGICs Tooltip Ligand gated ion channels


Stub icon

This analgesic-related article is a stub. You can help Wikipedia by expanding it.

AltStyle によって変換されたページ (->オリジナル) /