Home Cart Sign in  
Chemical Structure| 1188296-52-7 Chemical Structure| 1188296-52-7

Structure of PF-4800567
CAS No.: 1188296-52-7

Chemical Structure| 1188296-52-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

PF-4800567 is an inhibitor of casein kinase 1ε (CK1ε) with IC50 of 32 nM.

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of PF-4800567

CAS No. :1188296-52-7
Formula : C17H18ClN5O2
M.W : 359.81
SMILES Code : NC1=C2C(N(C3CCOCC3)N=C2COC4=CC=CC(Cl)=C4)=NC=N1
MDL No. :MFCD22123245
InChI Key :AUMDBEHGJRZSOO-UHFFFAOYSA-N
Pubchem ID :53472153

Safety of PF-4800567

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of PF-4800567

DNA
Hedgehog

Isoform Comparison

Biological Activity

Target
  • CK1

    casein kinase 1 epsilon, IC50:32 nM

    casein kinase 1 delta, IC50:711 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
WT SCN slices WT SCN slices no significant effect on circadian period Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
Ck1ε−/− SCN slices Ck1ε−/− SCN slices no significant effect on circadian period Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
Ck1εtau SCN slices Ck1εtau SCN slices significant lengthening of circadian period Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
Ck1ε−/− lung fibroblasts Ck1ε−/− lung fibroblasts no significant lengthening of circadian period (0.3 ±0.3 h) Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
Ck1εtau mutant lung fibroblasts Ck1εtau mutant lung fibroblasts slight lengthening of circadian period Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
WT lung fibroblasts WT lung fibroblasts slight lengthening of circadian period (0.9 ±0.13 h), but no significant effect in Ck1ε−/− cells (0.3 ±0.3 h) Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
HT1080 cells HT1080 cells Test the effect of PF4800567 on cell proliferation Oncogene. 2011 Jun 2;30(22):2558-69.
HEK293 cells HEK293 cells Test the effect of PF4800567 on cell proliferation Oncogene. 2011 Jun 2;30(22):2558-69.
HEK293STF3A cells HEK293STF3A cells Test the inhibitory effect of PF4800567 on Wnt/β-catenin signaling Oncogene. 2011 Jun 2;30(22):2558-69.
HEK293STF3A cells HEK293STF3A cells Test the inhibitory effect of PF4800567 on CK1ε autophosphorylation Oncogene. 2011 Jun 2;30(22):2558-69.
Mouse suprachiasmatic nucleus (SCN) organotypic slice cultures Mouse suprachiasmatic nucleus (SCN) organotypic slice cultures By inhibiting CK1ε activity, the short period of CK1εTau/Tau mutant was restored to the wild-type 24 h period, revealing the critical role of CK1ε in the SCN clock. J Neurosci. 2016 Sep 7;36(36):9326-41.
U87MG cells U87MG cells PF-4800567 had a modest effect on the viability of U87MG cells with an IC50 of approximately 28.4 μM Sci Rep. 2018 Sep 11;8(1):13621.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice WT, Ck1εtau mutant, and Ck1ε−/− mice Subcutaneous injection 100 mg/kg Daily injections for 10 days No significant effect on the period or phase of behavioral rhythms in WT or Ck1ε?/? mice, but significant period lengthening in Ck1εtau mutant mice Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15240-5.
Mice B6.B6Csnk1e and B6.D2Csnk1e mice Intraperitoneal injection 40 mg/kg Single administration PF-4800567 increased methamphetamine- and fentanyl-induced locomotor activity Neuropsychopharmacology. 2012 Mar;37(4):1026-35

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.78mL

0.56mL

0.28mL

13.90mL

2.78mL

1.39mL

27.79mL

5.56mL

2.78mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

Historical Records

Categories