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Redafamdastat

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(Redirected fromPF-04457845)
Chemical compound
Pharmaceutical compound
Redafamdastat
Clinical data
Other namesJZP-150; JZP150; PF-04457845; PF-4457845; PF04457845; PF4457845
Routes of
administration
By mouth
ATC code
  • None
Legal status
Legal status
Pharmacokinetic data
MetabolismCY3A4
Identifiers
  • N-pyridazin-3-yl-4-[(3-[5-(trifluoromethyl)pyridin-2-yl]oxyphenyl)methylidene]piperidine-1-carboxamide
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC23H20F3N5O2
Molar mass455.441 g·mol−1
3D model (JSmol)
  • n4ncccc4NC(=O)N(CC3)CC\C3=C/c2cc(ccc2)Oc(cc1)ncc1C(F)(F)F
  • InChI=1S/C23H20F3N5O2/c24-23(25,26)18-6-7-21(27-15-18)33-19-4-1-3-17(14-19)13-16-8-11-31(12-9-16)22(32)29-20-5-2-10-28-30-20/h1-7,10,13-15H,8-9,11-12H2,(H,29,30,32)
  • Key:BATCTBJIJJEPHM-UHFFFAOYSA-N

Redafamdastat (INNTooltip International Nonproprietary Name; developmental code namesJZP-150,PF-04457845) is aninhibitor of theenzymefatty acid amide hydrolase (FAAH), with anIC50Tooltip half-maximal inhibitory concentration of 7.2 nM, and bothanalgesic andanti-inflammatory effects inanimal studies comparable to those of thecyclooxygenase inhibitornaproxen.[1] It was being developed byJazz Pharmaceuticals for the treatment ofalcoholism,pain, andpost-traumatic stress disorder (PTSD) and reachedphase 2clinical trials.[2][3] However, development of the drug was discontinued in December 2023.[2]

See also

[edit]

References

[edit]
  1. ^Johnson DS, Stiff C, Lazerwith SE, Kesten SR, Fay LK, Morris M, et al. (February 2011)."Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor".ACS Medicinal Chemistry Letters.2 (2):91–96.doi:10.1021/ml100190t.PMC 3109749.PMID 21666860.
  2. ^ab"JZP 150".AdisInsight. 26 December 2023. Retrieved16 August 2024.
  3. ^"A Study of JZP150 in Adults With Posttraumatic Stress Disorder - Full Text View - ClinicalTrials.gov".clinicaltrials.gov.
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