Borrelidin

Borrelidin

CAT N°: 14436
Price:

From 231.00 196.35

Borrelidin is a secondary metabolite produced by Streptomyces and other bacteria. It displays potent antiangiogenic activity, preventing tube formation in rat aorta explants (IC50 = 0.8 nM) and inducing apoptosis in endothelial cells.{22549,22545} Borrelidin also alters the splicing of VEGF mRNA, producing an antiangiogenic isoform of the growth factor.{22550} It has long been known as a powerful inhibitor of both eukaryotic and bacterial threonyl tRNA synthetase.{22547} Borrelidin is also an effective anti-malarial drug, as it kills P. falciparum with an IC50 value of 1.8 nM.{22546} At higher doses, it inhibits cyclin-dependent kinase in yeast (IC50 = 24 ?M), resulting in growth arrest in the G1 phase.{22548}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (1R)-2R-[7-cyano-8R,16S-dihydroxy-9S,11R,13S,15S-tetramethyl-18-oxooxacyclooctadeca-4E,6Z-dien-2S-yl]-cyclopentanecarboxylic acid
  • Correlated keywords
    • 1403-11-8 97328-74-0 t-RNA synthetase anti-malarial plasmodium G-1 NSC216128
  • Product Overview:
    Borrelidin is a secondary metabolite produced by Streptomyces and other bacteria. It displays potent antiangiogenic activity, preventing tube formation in rat aorta explants (IC50 = 0.8 nM) and inducing apoptosis in endothelial cells.{22549,22545} Borrelidin also alters the splicing of VEGF mRNA, producing an antiangiogenic isoform of the growth factor.{22550} It has long been known as a powerful inhibitor of both eukaryotic and bacterial threonyl tRNA synthetase.{22547} Borrelidin is also an effective anti-malarial drug, as it kills P. falciparum with an IC50 value of 1.8 nM.{22546} At higher doses, it inhibits cyclin-dependent kinase in yeast (IC50 = 24 ?M), resulting in growth arrest in the G1 phase.{22548}

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