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Home > Products >  Organic Intermediate Toradol Powder CAS 74103-07-4 Ketorolac Tromethamine / Toradol

Organic Intermediate Toradol Powder CAS 74103-07-4 Ketorolac Tromethamine / Toradol CAS NO.74103-07-4

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Keywords

  • Toradol
  • 74103-07-4
  • Ketorolac Tromethamine

Quick Details

  • ProName: Organic Intermediate Toradol Powder CA...
  • CasNo: 74103-07-4
  • Molecular Formula: C19H24N2O6
  • Appearance: White powder
  • Application: Ketorolac is indicated for short-term ...
  • DeliveryTime: Abiut 10 days
  • PackAge: Aluminum foil bag,fluorinated bottles,...
  • Port: Shenzhen port
  • Purity: 99%
  • Storage: Store in cool & dry place. Keep away f...
  • Transportation: 1) Door to Door Service by DHL/FEDEX/E...
  • LimitNum: 0
  • Moisture Content: <0.1%
  • Impurity: <0.1%

Superiority

1) Provide costomers with "one-stop"packaging service,from research,development,production,export and so on.
2) We have our own R&D and production base,equipped with advanced production equipment and precision testing the Unitef States Pharmacopoeia(USP),the Britis Pharmacopoeia(EP) and other international advanced standards.All products are through the KOSGER,HALAL certification,the ISO quality management system certification and the HACCP certification.
3) More than 12 years of export experience.
4)Competitive price in China market.

Details

Ketorolac (tromethamine salt) inhibits both isoforms of Cox in recombinant rat and human enzyme systems. Ketorolac inhibits rat Cox-1 (IC50 of 0.27 μM), rat Cox-2 (IC50 of 2.06 μM), human Cox-1 (IC50 of 1.23 μM) and human Cox-2 (IC50 of 3.50 μM). The (S) enantiomer of Ketorolac with rat Cox-1 (IC50 of 0.10 μM) is approximately twice as potent as the racemate, whereas the (R)-enantiomer (IC50 of > 100 μM) is virtually without activity. Ketorolac shows inhibition of eicosanoid formation in HEL cells (Cox-1, IC50 of 0.025 μM) and LPS-stimulated Mono Mac 6 cells (Cox-2, IC50 of 0.039 μM), 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 cycle at G0/G1 phase in hOBs.

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