7-oxo Staurosporine

7-oxo Staurosporine

CAT N°: 23346
Price:

From 488.00 414.80

7-oxo Staurosporine is an antibiotic originally isolated from S. platensis with diverse biological activites.{41405,41406,41407,41409} It inhibits PKC, PKA, phosphorylase kinase, EGFR, and c-Src in vitro (IC50s = 9, 26, 5, 200, and 800 nM, respectively).{41406} 7-oxo Staurosporine induces cell cycle arrest in the G2/M phase in human leukemia K562 cells with a minimal effective dose (MED) of 30 ng/ml.{41405} It is cytotoxic to P388 mouse leukemia cells that are resistant and susceptible to doxorubicin (Item No. 15007; IC50s = 27 and 45 nM, respectively).{41407} 7-oxo Staurosporine inhibits growth of the mycelial, but not yeast form of C. albicans, C. krusei, C. tropicalis, and C. lusitaniae (MICs = 3.1-25 ?g/ml).{41408} It increases sphingomyelin synthesis in CHO-K1 cells when used at a concentration of 50 nM.{41409}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (9S,10R,11R,13R)-10,11,12,13-tetrahydro-10-methoxy-9-methyl-11-(methylamino)-9,13-epoxy-1H,9H-diindolo[1,2,3-gh:3′,2′,1′-lm]pyrrolo[3,4-j][1,7]benzodiazonine-1,3(2H)-dione
  • Correlated keywords
    • 141196-69-2 BMY41950 RK1409 Oxostaurosporine anti-biotic CHOK1
  • Product Overview:
    7-oxo Staurosporine is an antibiotic originally isolated from S. platensis with diverse biological activites.{41405,41406,41407,41409} It inhibits PKC, PKA, phosphorylase kinase, EGFR, and c-Src in vitro (IC50s = 9, 26, 5, 200, and 800 nM, respectively).{41406} 7-oxo Staurosporine induces cell cycle arrest in the G2/M phase in human leukemia K562 cells with a minimal effective dose (MED) of 30 ng/ml.{41405} It is cytotoxic to P388 mouse leukemia cells that are resistant and susceptible to doxorubicin (Item No. 15007; IC50s = 27 and 45 nM, respectively).{41407} 7-oxo Staurosporine inhibits growth of the mycelial, but not yeast form of C. albicans, C. krusei, C. tropicalis, and C. lusitaniae (MICs = 3.1-25 ?g/ml).{41408} It increases sphingomyelin synthesis in CHO-K1 cells when used at a concentration of 50 nM.{41409}

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