PF-04859989 HCl

CAS No. 177943-33-8

PF-04859989 HCl( PF-04859989HCl | PF-04859989 | PF 04859989 | PF04859989 )

Catalog No. M27913 CAS No. 177943-33-8

PF-04859989 HCl is a brain-penetrable and irreversible inhibitor of kynurenine amino transferase II (KAT II), which is the enzyme responsible for most of the brain synthesis of kynurenic acid.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 63 In Stock
2MG 36 In Stock
5MG 57 In Stock
10MG 93 In Stock
25MG 180 In Stock
50MG 276 In Stock
100MG 454 In Stock
200MG 634 In Stock
500MG 986 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PF-04859989 HCl
  • Note
    Research use only, not for human use.
  • Brief Description
    PF-04859989 HCl is a brain-penetrable and irreversible inhibitor of kynurenine amino transferase II (KAT II), which is the enzyme responsible for most of the brain synthesis of kynurenic acid.
  • Description
    PF-04859989 HCl is a brain-penetrable and irreversible inhibitor of kynurenine amino transferase II (KAT II), which is the enzyme responsible for most of the brain synthesis of kynurenic acid.(In Vitro):The IC50s values are 23 and 263 nM for hKAT II and rKAT II. PF-04859989 HCl is selective for KAT II over human KAT I, KAT III, and KAT IV (IC50s of 22, 11, and >50 μM, respectively).(In Vivo):Acute administration of the KAT II inhibitor PF-04859989 (5 or 10 mg/kg) was associated with a short-onset, time-dependent decrease in firing rate and burst activity of DA neurons, both parameters reaching a 50% reduction within 45 min. Furthermore, PF-04859989 reduced the number of spontaneously active DA cells as measured 4-6 after administration. Pretreatment with d-cycloserine (30 mg/kg) or CGP-52432 (10 mg/kg) prevented the inhibitory action of PF-04859989 (5 mg/kg) on firing rate and burst firing activity. In contrast, pretreatment with methyllycaconitine (MLA, 4 mg/kg) did not change the response, whereas picrotoxin (4.5 mg/kg) partially prevented the inhibitory effects of PF-04859989 (5 mg/kg, i.v.).
  • In Vitro
    ——
  • In Vivo
    In vivo pharmacokinetic and efficacy studies in rat show that PF-04859989 is a brain-penetrant, irreversible inhibitor and is capable of reducing brain kynurenic acid by 50% at a dose of 10 mg/kg (sc). Rats receiving PF-04859989 (5 mg/kg; i.p.) exhibited a significantly lower number of spontaneously active DA neurons pertrack. Animal Model:Male Sprague-Dawley ratsDosage:5 mg/kg Administration:I.p.Result:Exhibited a significantly lower number of spontaneously active dopamine (DA) neurons pertrack compared to controls.
  • Synonyms
    PF-04859989HCl | PF-04859989 | PF 04859989 | PF04859989
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    myeloperoxidase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    177943-33-8
  • Formula Weight
    286.93
  • Molecular Formula
    C7H6BrCl2NO2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 100 mg/mL (465.87 mM)
  • SMILES
    Cl.[O-][N+](=O)c1cccc(Cl)c1CBr
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Arvadia P, et al. 4-Aminobenzoic acid hydrazide inhibition of microperoxidase-11: catalytic inhibition by reactive metabolites. Arch Biochem Biophys. 2011 Nov;515(1-2):120-6.
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