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Medchemexpress LLC JBI-589 | 2308504-22-3 | C29H28FN5O | 1 ML
SDP

Catalog No. 5000373189
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JBI-589 is a non-covalent, orally bioavailable, isoform-selective inhibitor of PAD4 (Protein Arginine Deiminase 4). It is suitable for use in cancer research, as it has been shown to reduce CXCR2 expression and block neutrophil chemotaxis, while also reducing primary tumor and metastases. This compound can enhance the anti-tumor effects of checkpoint inhibitors.

  • Significantly downregulates CXCR2 expression on neutrophils
  • Reduces CXCL1-induced migration
  • Inhibits citrullination of histone H3 in induced mouse neutrophils
  • Significantly inhibits primary tumor growth in mouse models
  • Leads to a significant downregulation of CXCR2 receptor expression in Ly6G cells

Catalog No. 50-003-73189 Supplier Medchemexpress LLC Supplier No. HY15345010MM/1ML
May include imposed supplier surcharges.
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JBI-589 is a non-covalent, orally bioavailable, isoform-selective inhibitor of PAD4 (Protein Arginine Deiminase 4). It is suitable for use in cancer research, as it has been shown to reduce CXCR2 expression and block neutrophil chemotaxis, while also reducing primary tumor and metastases. This compound can enhance the anti-tumor effects of checkpoint inhibitors.

  • Significantly downregulates CXCR2 expression on neutrophils
  • Reduces CXCL1-induced migration
  • Inhibits citrullination of histone H3 in induced mouse neutrophils
  • Significantly inhibits primary tumor growth in mouse models
  • Leads to a significant downregulation of CXCR2 receptor expression in Ly6G cells

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