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ERK Inhibitor

Catalog No.
C4096
Selectively inhibits ERK2, blocking downstream phosphorylation of Rsk-1 and Elk-1.
Grouped product items
SizePriceStock Qty
500ug
$96.00
In stock
1mg
$115.00
In stock
5mg
$189.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

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Background

ERK Inhibitor (CAS No.: 1049738-54-6) is a small-molecule modulator of the extracellular signal-regulated kinase (ERK) signaling pathway that exhibits preferential binding to the ERK2 isoform, with reported binding affinity in the low micromolar range. It functions by selectively inhibiting the phosphorylation of downstream ERK substrates, including Rsk-1 and Elk-1, thereby disrupting ERK-mediated signal transduction while exerting minimal influence on ERK phosphorylation by upstream kinases such as MEK1/2. This selective mechanism makes it a valuable tool for dissecting ERK-dependent cellular processes, including proliferation, differentiation, and survival, without broadly suppressing upstream pathway activation. As a research reagent, it is commonly utilized in biochemical and cell-based assays to investigate ERK pathway dynamics, validate target engagement, and support early-stage drug discovery efforts focused on mitogen-activated protein kinase signaling. Experimental concentrations typically fall within the micromolar range, although precise dosing conditions vary depending on the specific cellular context and study design.

Chemical Properties

Physical AppearanceA crystalline solid
Storage-20°C
M.Wt328.06
Cas No.1049738-54-6
FormulaC14H17ClN2O3S
SynonymsExtracellular Regulated Kinase Inhibitor
Solubility≤2mg/ml in DMSO
Chemical Name(Z)-3-(2-aminoethyl)-5-(4-ethoxybenzylidene)thiazolidine-2,4-dione hydrochloride
Canonical SMILESCCOC1=CC=C(/C=C2SC(N(CCN)C\2=O)=O)C=C1.Cl
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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