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Ketorolac Chemical Structure

Ketorolac

Data Sheet For research use only. Not for human use.
Cat. No. :BCP02917CAS No. :74103-07-4Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 74103-07-4 Cat. No. BCP02917
Name Ketorolac
Synonyms Toradol;Ketorolac tromethamine;
SMILES
Chemical Name
Formula C19H24N2O6 M. Wt 376.4
Purity 98% Storage Store at 4-8°C
Description (R, S)-, (S)-, and (R)-Ketorolac inhibit both isoforms of COX in recombinant rat and human enzyme systems, and similar as inhibitors of rat COX (rCOX) and human COX (hCOX) under the conditions used. (R, S)-Ketorolac inhibits rat COX-1, rat COX-2, human COX-1 and human COX-2 with IC50 of 0.27 μM, 2.06 μM, 1.23 μM and 3.50 μM, respectively. The (S) enantiomer of Ketorolac with IC50 of 0.10 μM for rat COX-1 is approximately twice as potent as the racemate, whereas the (R)-enantiomer with IC50 of > 100 μM is virtually without activity.Ketorolac shows inhibition of eicosanoid formation in HEL cells (COX-1) and LPS-stimulated Mono Mac 6 cells (COX-2) with IC50 of 0.025 μM and 0.039 μM, respectively, but does not significantly inhibit NO accumulation in supernatants of LPS-stimulated RAW 264.7 cells up to 300 μM. Ketorolac significantly inhibits thymidine incorporation of human osteoblasts (hOBs) upon 24 hours treatment in a dose-dependent manner, and inhibits proliferation and arrests cell c
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