PD 98059

貨號 Cat. No.
P-260
規格 Size
10 x 0.1 mg 1mg 5x1mg

Description

PD 98059


Potent Inhibitor of Mitogen-Activated Protein Kinase  (MAPK) Pathway











Product#: P-260

























Sizes:
10 x 0.1 mg
1 mg
5 x 1 mg
 
 
 





is a synthetic flavonoid and a potent inhibitor of mitogen-activated protein kinase (MAPK) by inhibiting its immediate upstream activator, mitogen activated protein kinase kinase (also known as MEK or MKK1).1-3

PD 98059 arrests cell cycle progression of some rat cultured cells at the G0/G1 phase and blocks nerve growth factor stimulated axonal outgrowth from adult mouse dorsal root ganglia in vitro,4-5 and blocks induction of LTP in the brain areas.6-7


PD 98059 is also an equipotent antagonist of aryl hydrocarbon receptor (AHR) stimulated by TCDD in MCF10A cells, 8-10


 











M.W.: 360.21










CAS No.: [167869-21-8]












Structure:
 








 










Purity: >99%












Bioassay:
PD 98059 inhibits phophorylation of P42/44 MAPK (ERK) stimulated by PDGF.











C6 glioma cells were grown to 70% confluence and then serum starved for 1.5 h. The cells were incubated for 2 h with various concentrations of PD 98059 as indicated in the picture and stimulated with 7ng/ml PDGF-AA. The cell proteins were resolved by SDS PAGE and probed with anti-phospho-P42/44 MAPK (upper panel), stripped and followed by reprobing with anti-P42/44 MAPK (lower panel). The inhibition of P42/44 MAPK phosphorylation by PD 98059 is dose dependent.









 









References:














































1.



Alessi, D.R., et al. (1995) J. Biol. Chem.  270, 27489.



2.



Dudley, D.T., et al. (1995) Proc. Natl. Acad. Sci.  92, 7686.



3.



Pang, L. et al. (1995) J. Biol. Chem. 270, 13585.



4.



Yamaguchi, K. et al. (2002) J. Ophthalmol. 46, 634.



5.



Sjogreen, B. et al. (2000) Neuroscience 100, 407.



6.



Andrew, N. et al. (1999) J. Neurophysiol. 81, 103.



7.



English, J. D. et al. (1997) J. Biol. Chem. 272, 19103.



8.



Guyton, K.Z. et al. (1996) Cancer Res.  36, 3480.



9.



Cook, S.J. et al. (1997) J. Biol. Chem.  272,13309.



10.



John, J. et al. (1998) Mol. Pharmacol. 53, 438.




PD 98059

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