Description
SC-58125 is a potent and selective inhibitor of cyclooxygenase 2 (COX-2), with an IC50 of 0.04 μM. SC-58125 exhibits antitumor activity in vitro and in vivo. SC-58125 also can inhibit edema at the inflammatory site and has analgesic effect.
Product information
CAS Number: 162054-19-5
Molecular Weight: 384.35
Formula: C17H12F4N2O2S
Chemical Name: 5-(4-fluorophenyl)-1-(4-methanesulfonylphenyl)-3-(trifluoromethyl)-1H-pyrazole
Smiles: CS(=O)(=O)C1C=CC(=CC=1)N1N=C(C=C1C1=CC=C(F)C=C1)C(F)(F)F
InChiKey: JHBIMJKLBUMNAU-UHFFFAOYSA-N
InChi: InChI=1S/C17H12F4N2O2S/c1-26(24,25)14-8-6-13(7-9-14)23-15(10-16(22-23)17(19,20)21)11-2-4-12(18)5-3-11/h2-10H,1H3
Technical Data
Appearance: Solid Power
Purity: ≥98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis
Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.
Shelf Life: ≥12 months if stored properly.
Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.
Drug Formulation: To be determined
HS Tariff Code: 382200
How to use
In Vitro:
SC-58125 (0.001-100 μM) has a high degree of selectivity for the inducible form of COX-2 (IC50=1 μM) over the COX-1 (IC50>100 μM). SC-58125 (10 μM; 20-140 s) is time-dependent and is complete by 1 min, with a half-maximal inhibition at 20 s. SC-58125 (25-100 μM; 3 d) inhibits the in vitro growth of HCA-7 and LLC cells. SC-58125 (100 µM; 12 h) induces G2 arrest in LLC cells. SC-58125 (25-100 μM; 3 d) decreases p34cdc2 levels in HCA-7 cells. SC-58125 (100 µM; 24 or 72 h) does not induce apoptosis of HCA-7 and LLC cells.
In Vivo:
SC-58125 (10 mg/kg; i.p. every 48 h) inhibits the growth of established colorectal cancer xenografts in mice. SC-58125 (10 mg/kg; a single i.p.) reduces tumor PGE2 levels in mice. SC-58125 (10 mg/kg; a single i.p.) does not change the tumor levels of COX-1 and COX-2 protein in mice.
Products are for research use only. Not for human use.
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