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PF-4950834

Chemical Structure : PF-4950834

CAS No.: 1256264-62-6

PF-4950834 (PF4950834;PF 4950834)

Catalog No.: PC-60681Not For Human Use, Lab Use Only.

PF-4950834 is a potent, selective, ATP-competitive and orally acitve Rho kinase (ROCK) inhibitor with IC50 of 33.1 and 8.5 nM for ROCK1 and ROCK2, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

PF-4950834 is a potent, selective, ATP-competitive and orally acitve Rho kinase (ROCK) inhibitor with IC50 of 33.1 and 8.5 nM for ROCK1 and ROCK2, respectively.
PF-4950834 displays 5-140-fold selectivity over other AGC kinase family.
PF-4950834 inhibits Jurkat T cell migration with IC50 of 68.4 nM, suppresses activation of both LPA- and thrombin-mediated activation of Rho kinase, and blocked both LPA-induced and thrombin-induced expression of ICAM-1 and VCAM-1 in HUVECs.
PF-4950834 attenuates leukocyte migration in vivo.

Physicochemical Properties

M.Wt 345.402
Formula C21H19N3O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-methyl-3-{[(4-pyridin-4-ylbenzoyl)amino]methyl}benzamide

References

1. Rajagopalan LE, et al. J Pharmacol Exp Ther. 2010 Jun;333(3):707-16.

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