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AZ10397767 

Cat. No. M29932

All AbMole products are for research use only, cannot be used for human consumption.

AZ10397767  Structure

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Quality Control & Documentation
Biological Activity

AZ10397767 is an orally active, selective CXCR2 receptor antagonist with an IC50 of 1 nM. AZ10397767 attenuates the Oxaliplatin-induced NF-κB transcriptional activity and potentiates Oxaliplatin-induced apoptosis in androgen-independent prostate cancer (AIPC) cells. AZ10397767 significantly inhibits neutrophil recruitment into tumors which then adversely affects tumor growth in vitro and in vivo.

Chemical Information
Molecular Weight 400.88
Formula C15H14ClFN4O2S2
CAS Number 333742-63-5
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
References

[1] Catherine Wilson, et al. PLoS One. Constitutive and treatment-induced CXCL8-signalling selectively modulates the efficacy of anti-metabolite therapeutics in metastatic prostate cancer

[2] Simon Tazzyman, et al. Int J Cancer. Inhibition of neutrophil infiltration into A549 lung tumors in vitro and in vivo using a CXCR2-specific antagonist is associated with reduced tumor growth

[3] A Seaton, et al. Br J Cancer. Inhibition of constitutive and cxc-chemokine-induced NF-kappaB activity potentiates ansamycin-based HSP90-inhibitor cytotoxicity in castrate-resistant prostate cancer cells

[4] Catherine Wilson, et al. Mol Cancer Ther. Interleukin-8 signaling attenuates TRAIL- and chemotherapy-induced apoptosis through transcriptional regulation of c-FLIP in prostate cancer cells

[5] Angela Seaton, et al. Carcinogenesis. Interleukin-8 signaling promotes androgen-independent proliferation of prostate cancer cells via induction of androgen receptor expression and activation

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Keywords: AZ10397767  supplier, CXCR, inhibitors, activators

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