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Ketoprofen COX inhibitor

Cat.No.S1645

Ketoprofen (RP-19583) is a dual COX1/2 inhibitor, used as a nonsteroidal anti-inflammatory drug to treat arthritis-related inflammatory pains.
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Quality Control

Batch: Purity: 100%
100

Solubility

In vitro
Batch:

DMSO : 51 mg/mL (200.56 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 51 mg/mL

Water : Insoluble

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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Chemical Information, Storage & Stability

Molecular Weight 254.28 Formula

C16H14O3

Storage (From the date of receipt)
CAS No. 22071-15-4 Download SDF Storage of Stock Solutions

Synonyms RP-19583 SMILES CC(C1=CC(=CC=C1)C(=O)C2=CC=CC=C2)C(=O)O

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
COX-1
COX-2
In vitro
Ketoprofen combined with UVB irradiation induces the cytotoxicity and suppresses DNA synthesis in HaCaT cells in a concentration-dependent manner. This compound combined with UVB irradiation inhibits the cell growth and induces G2/M cell cycle arrest by modulating the levels of cdc2, cyclin B1, Chk1, Tyr15-phosphorylated cdc2 and p21. It also provokes a striking accumulation of cyclin B1-cdc2-p21 complexes, concomitantly with an increase in the levels of Tyr15-phosphorylated cdc2 and p21 protein. This chemical combined with UVB irradiation accentuates the apoptotic response to UVB radiation in HaCaT cells as evidenced by DAPI staining.
In vivo
Ketoprofen at 1% level in suitable topical vehicles can effectively inhibit GCF-LTB4 and GCF-PGE2 and positively alter alveolar bone activity in the ligature-induced model of periodontitis in the monkey. This compound (3.63 mg/kg bwt) reduces hoof pain andlameness to a greater extent than the 2.2 mg/kg dose and phenylbutazone. It is more effective than local anesthesia (LA), or caudal epidural anesthesia (EPI) in decreasing cortisol and partially reverses the reduction in average daily gain (ADG) following castration. This chemical (40 and 80 mg/kg diet) reduces the incidence of transitional cell carcinoma of the urinary bladder by >70% from that seen in dietary mice.
References
  • [4] https://pubmed.ncbi.nlm.nih.gov/12772856/
  • [5] https://pubmed.ncbi.nlm.nih.gov/8706245/

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-07-24)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06912763 RECRUITING
Fibrosis Syndrome; Lymphedema; Head &Amp; Neck Cancer; Fibrosis
M.D. Anderson Cancer Center
2025-08-08 PHASE2
NCT05584046 RECRUITING
Plantar Fasciitis
Chinese University of Hong Kong
2023-09-20
NCT06731647 RECRUITING
Non-steroidal Anti-inflammatory Drugs; Pleurodesis; Pneumothorax; Pain Management
Centre Hospitalier Universitaire, Amiens
2025-02-01 PHASE2
NCT06381063 RECRUITING
Acute Postoperative Pain; Non-steroidal Anti-inflammatory Drugs; Cardiac Surgery; Pain Intensity; Multimodal Pain Management
Centre Hospitalier Universitaire, Amiens
2024-03-27 PHASE3
NCT07319728 ACTIVE_NOT_RECRUITING
Knee Osteoarthritis
New Valley University
2025-05-10 PHASE1
NCT07610265 COMPLETED
Post Endodontic Pain
Nims University Rajasthan
2024-04-18 PHASE4

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