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DSP-2230

From Wikipedia, the free encyclopedia
Investigational analgesic drug
This article needs to beupdated. Please help update this article to reflect recent events or newly available information.(October 2024)
Pharmaceutical compound
DSP-2230
Clinical data
Routes of
administration
By mouth
Identifiers
  • (2S)-2-[[[3-cyclobutyl-5-(3,4,5-trifluorophenoxy)-3H-imidazo[4,5-b]pyridin-2-yl]methyl]amino]propanamide
CAS Number
UNII
ChEMBL
Chemical and physical data
FormulaC20H20F3N5O2
Molar mass419.408 g·mol−1
3D model (JSmol)
  • FC1=CC(OC2=CC=C(N=C3CN([C@@H](C(N([H])[H])=O)C)[H])C(N3C4CCC4)=N2)=CC(F)=C1F
  • InChI=1S/C20H20F3N5O2/c1-10(19(24)29)25-9-16-26-15-5-6-17(27-20(15)28(16)11-3-2-4-11)30-12-7-13(21)18(23)14(22)8-12/h5-8,10-11,25H,2-4,9H2,1H3,(H2,24,29)/t10-/m1/s1
  • Key:HHXCJIMPEJSJTG-SNVBAGLBSA-N

DSP-2230 is aselectivesmall-moleculeNav1.7 andNav1.8voltage-gated sodium channelblocker which is under development byDainippon Sumitomo Pharma for the treatment ofneuropathic pain.[1][2] As of June 2014, it is inphase I/phase IIclinical trials.[1][2]

See also

[edit]

References

[edit]
  1. ^abMartz L (2014)."Nav-i-gating antibodies for pain".Science-Business EXchange.7 (23): 662.doi:10.1038/scibx.2014.662.ISSN 1945-3477.
  2. ^abBagal 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):3690–9.doi:10.1016/j.bmcl.2014.06.038.PMID 25060923.

External links

[edit]
  • "DSP-2230".AdisInsight. Springer Nature Switzerland AG.
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
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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