A potent and highly selective human CCR2 (hCCR2) antagonist (IC50 = 3.7 nM, 4.7 nM, and 84 nM for monocyte chemoattractant protein-1 binding to hCCR2, chemotaxis activity, inhibition of the hERG potassium current, respectively).
Biochem/physiol Actions
Primary Target human CCR2 (hCCR2)
Target IC50: 3.7 nM, 4.7 nM, and 84 nM for different assays.
Warning
Toxicity: Standard Handling (A)
Reconstitution
Following reconstitution, aliquot and freeze 9-20°C). Stock solutions are stable for up to 3 months at -20°C.
Other Notes
Xia, M., et al. 2009. Expert Opinion on Therapeutic Patents.19, 295.
Xue, C., et al. 2011. ACS Med. Chem. Lett.2, 450.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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