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Pd 184352

Manufactured by Cell Signaling Technology
Sourced in Germany

PD-184352 is a potent and selective inhibitor of the mitogen-activated protein kinase kinase (MEK1/2). It functions by blocking the activation of ERK1/2, which are key components of the Ras/Raf/MEK/ERK signaling pathway.

Automatically generated - may contain errors

2 protocols using pd 184352

1

Inhibitor Evaluation of Cardiovascular Markers

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Unless stated otherwise, all reagents were from Merck (Darmstadt, Germany). Inhibitors used were: CGS35066, an ECE-1 inhibitor (Tocris Bioscience/Bio-Techne; Wiesbaden, Germany); valsartan, an angiotensin receptor type I (AT1) antagonist (Sigma-Aldrich; Schnelldorf, Germany, Merck, Darmstadt, Germany); PD-184352, an inhibitor of extracellular signal-regulated kinases (ERK) (Cell Signaling Technology, Danvers, MA, USA); and PEG-SOD, a superoxide dismutase-polyethylene glycol conjugate (Sigma-Aldrich®, Merck). Their effective concentrations were determined in preliminary experiments.
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2

Small Molecule Inhibitors in Cell Signaling

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The following small molecule inhibitors were used in this study: MEK inhibitors: 2 μM PD 184352 (Cell Signaling 12147) and 10 μM Selumetinib (Selleckchem S1008), ERK inhibitor: 10 μM GDC-0994 (Selleckchem S755403), PI3k inhibitor: 2 μM ZSTK474 (Selleckchem S1072), ROCK inhibitors: 25 μM Y-27632 (Sigma Y0503) and 2 μM GSK 269962 (Tocris 4009). Details of treatment times are described in figure legends.
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