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Ketorolac (tromethamine salt) inhibits both isoforms of Cox in recombinant rat and human enzyme systems. Ketorolac inhibits rat Cox-1 (IC50 of 0.27 muM), rat Cox-2 (IC50 of 2.06 muM), human Cox-1 (IC50 of 1.23 muM) and human Cox-2 (IC50 of 3.50 muM). The (S) enantiomer of Ketorolac with rat Cox-1 (IC50 of 0.10 muM) is approximately twice as potent as the racemate, whereas the (R)-enantiomer (IC50 of > 100 muM) is virtually without activity. Ketorolac shows inhibition of eicosanoid formation in HEL cells (Cox-1, IC50 of 0.025 muM) and LPS-stimulated Mono Mac 6 cells (Cox-2, IC50 of 0.039 muM), but does not significantly inhibit NO accumulation in supernatants of LPS-stimulated RAW 264.7 cells up to 300 muM. Ketorolac significantly inhibits thymidine incorporation of human osteoblasts (hOBs) upon 24 hours treatment in a dose-dependent manner, and inhibits proliferation and arrests cell cycle at G0/G1 phase in hOBs.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Ketorolac (tromethamine salt), 500 mg | sc-205360 | 500 mg | $20.00 | |||
Ketorolac (tromethamine salt), 1 g | sc-205360A | 1 g | $52.00 |