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JZP150 (formerly PF-04457845) is a potent and exquisitely selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), with an IC50 of 7.2nM, and both analgesic and antiinflammatory effects in animal studies comparable to naproxen. It has been well tolerated in human trials even at high dose ranges with no evidence for cognitive dysfunction, and has completed Phase II clinical trials for the treatment of osteoarthritis, but was found to be ineffective. JZP150 is currently being developed by Jazz Pharmaceuticals and is in a Phase 2 trial in the US for PTSD.

AttributesValues
rdf:type
rdfs:label
  • PF-04457845 (en)
rdfs:comment
  • JZP150 (formerly PF-04457845) is a potent and exquisitely selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), with an IC50 of 7.2nM, and both analgesic and antiinflammatory effects in animal studies comparable to naproxen. It has been well tolerated in human trials even at high dose ranges with no evidence for cognitive dysfunction, and has completed Phase II clinical trials for the treatment of osteoarthritis, but was found to be ineffective. JZP150 is currently being developed by Jazz Pharmaceuticals and is in a Phase 2 trial in the US for PTSD. (en)
foaf:name
  • JZP150 (en)
foaf:depiction
  • http://commons.wikimedia.org/wiki/Special:FilePath/PF-04457845_Structure.svg
dct:subject
Wikipage page ID
Wikipage revision ID
Link from a Wikipage to another Wikipage
sameAs
dbp:wikiPageUsesTemplate
thumbnail
ATC prefix
  • None (en)
c
CAS number
ChEMBL
ChemSpiderID
drug name
  • JZP150 (en)
F
H
IUPAC name
  • N-pyridazin-3-yl-4-[methylidene]piperidine-1-carboxamide (en)
legal US
  • Investigational New Drug (en)
metabolism
  • CY3A4 (en)
n
O
PubChem
SMILES
  • n4ncccc4NCNCC\C3=C/c2ccOcncc1CF (en)
StdInChI
StdInChIKey
  • BATCTBJIJJEPHM-UHFFFAOYSA-N (en)
UNII
  • H4C81M8YYW (en)
width
has abstract
  • JZP150 (formerly PF-04457845) is a potent and exquisitely selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH), with an IC50 of 7.2nM, and both analgesic and antiinflammatory effects in animal studies comparable to naproxen. It has been well tolerated in human trials even at high dose ranges with no evidence for cognitive dysfunction, and has completed Phase II clinical trials for the treatment of osteoarthritis, but was found to be ineffective. As of 2021, several studies have shown that this novel FAAH inhibitor may reduce cannabis withdrawal symptoms and cannabis use in men, and might represent an effective and safe approach for the treatment of cannabis use disorder. JZP150 is currently being developed by Jazz Pharmaceuticals and is in a Phase 2 trial in the US for PTSD. (en)
prov:wasDerivedFrom
page length (characters) of wiki page
CAS number
  • 1020315-31-4
ChEMBL
  • 1651534
FDA UNII code
  • H4C81M8YYW
PubChem
  • 24771824
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