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Cot inhibitor-2

This orally active small molecule is a potent and selective inhibitor of Cot (Tpl2/MAP3K8) with an IC50 of 1.6 nM. It effectively suppresses LPS-induced TNF-α production in human whole blood (IC50 = 0.3 μM), making it a valuable tool for investigating inflammatory signaling pathways in both cellular and animal models.

Product Specifications

CAS Number

915363-56-3

Product Name Alternative

Cot inhibitor 2, Cot inhibitor2, Cot inhibitor-2, COT/Tpl2, MAP3K, TNF-α

Field of Research

Cell Biology, Pharmacology & Drug Discovery, Signal Transduction

Purity

98.87% (May vary between batches)

Solubility

DMSO:40 mg/mL (74.15 mM) ;10% DMSO+40% PEG300+5% Tween 80+45% Saline:2.5 mg/mL (4.63 mM)

Smiles

CCN1CCC (CC1) n1cc (CNc2cc (Cl) c3ncc (C#N) c (Nc4ccc (F) c (Cl) c4) c3c2) nn1

Molecular Formula

C26H25Cl2FN8

Molecular Weight

539.43

Storage Conditions

-20°C

Notes

For research use only.

Available Sizes

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