Purvalanol A

Purvalanol A

CAT N°: 14579
Price:

From 48.00 40.80

Purvalanol A is a potent, cell-permeable, and selective inhibitor of cyclin-dependent kinases (CDKs) with IC50 values of 4, 70, 35, 850, and 75 nM for cdc2/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E, Cdk4/cyclin D1 and Cdk5-p35, respectively.{6960,14995} Purvalanol A reversibly arrests synchronized cells in the G1 and G2 phase of the cell cycle, inhibiting both cell proliferation and cell death.{22865} At 10 ?M, purvalanol A potently suppresses the anchorage-independent growth of c-Src-transformed cells as well as HT-29 and SW48 human colon cancer cells.{22866}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (2R)-2-[[6-[(3-chlorophenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-3-methyl-1-butanol
  • Correlated keywords
    • inhibitors cyclin-dependent kinases cyclins cdc2/cyclin B cec2 cyclins Cdk2/cyclin A Cdk2 Cdk2/cyclin E Cdk4/cyclin D1 Cdk4 Cdk5-p35 Cdk5 p35 cells cycles proliferations cancers purvalanol-A potent permeables cell-permeable inhibits inhibitions deaths c-Src cSrc c Src HT29 HT-29 HTs 29 SW48 SW 48 SW-48 colons NG60 NGs 60 NG-60 arrests synchronized G1 G2 growths phases apoptosis anchorages independent anchorage-indenpendent transformed humans CDKs
  • Product Overview:
    Purvalanol A is a potent, cell-permeable, and selective inhibitor of cyclin-dependent kinases (CDKs) with IC50 values of 4, 70, 35, 850, and 75 nM for cdc2/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E, Cdk4/cyclin D1 and Cdk5-p35, respectively.{6960,14995} Purvalanol A reversibly arrests synchronized cells in the G1 and G2 phase of the cell cycle, inhibiting both cell proliferation and cell death.{22865} At 10 ?M, purvalanol A potently suppresses the anchorage-independent growth of c-Src-transformed cells as well as HT-29 and SW48 human colon cancer cells.{22866}

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