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Meloxicam COX inhibitor

Cat.No.S1734

Meloxicam is a selective COX inhibitor, used to relieve pain and fever effects.
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Quality Control

Batch: S173401 DMSO]30 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 99.91%
99.91

Solubility

In vitro
Batch:

DMSO : 30 mg/mL (85.37 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
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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.
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Chemical Information, Storage & Stability

Molecular Weight 351.4 Formula

C14H13N3O4S2

Storage (From the date of receipt)
CAS No. 71125-38-7 Download SDF Storage of Stock Solutions

Synonyms N/A SMILES CC1=CN=C(S1)NC(=O)C2=C(C3=CC=CC=C3S(=O)(=O)N2C)O

Read more about storage stability stock solution CAS number SMILES

Mechanism of Action

Targets/IC50/Ki
COX
In vitro
Meloxicam significantly reduces HCA-7 and Moser-S colony size. This compound significantly inhibits HCA-7 colony and tumor growth but has no effect on the growth of the COX-2 negative HCT-116 cells. It inhibits PGE(2) production, proliferation and invasiveness especially in MG-63 cells, which express relatively high levels of COX-2. This chemical causes apoptosis and upregulates Bax mRNA and protein in MG-63 cell culture.
In vivo
Meloxicam suppresses LM-8 tumor growth and lung metastasis in vivo mouse model. This compound causes a significant reduction in lameness at post injection hour (PIH) 8 and 24 and tends to reduce effusion in horse. It significantly suppresses synovial fluid (SF) prostaglandin E2 and substance P release at PIH 8 and bradykinin at PIH 24 compared to placebo treatment in horse. This agent reduces general MMP activity at PIH 8 and 24 in horse. This compound- or flunixin-treated horses has improved postoperative pain scores and clinical variables, compared with SS-treated horses. It results in high numbers of neutrophils in ischemia-injured tissue of horse. Its administration significantly suppresses PGE2 concentrations in blood and synovial fluid at days 7 and 21, but has no effect on concentrations of TXB2 in blood or PGE2 in gastric mucosa in dogs.
References
  • [4] https://pubmed.ncbi.nlm.nih.gov/17542694/
  • [5] https://pubmed.ncbi.nlm.nih.gov/12428662/

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2025-10-24)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT07158476 RECRUITING
ACL Surgery; Pain Management
St. Louis University
2025-10-21 PHASE4
NCT07430085 NOT_YET_RECRUITING
Periarticular Block; Osteoarthritis (OA); Osteoarthritis (OA) of the Knee; Pain After Surgery; Knee Arthroplasty, Total
Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
2026-07-31 PHASE4
NCT07743684 ACTIVE_NOT_RECRUITING
Temporomandibular Joint Internal Derangement
Hussein Mohammed Ridha
2026-01-01
NCT07775248 RECRUITING
Osteoarthritis (OA) of the Knee
Henry Ford Health System
2025-02-11 PHASE4
NCT07200544 RECRUITING
Postoperative Pain, Acute; Skin Cancer
University of Oklahoma
2025-10-15 PHASE4
NCT05644496 TERMINATED
Post Operative Pain; Osteoarthritis, Knee
Baptist Health South Florida
2023-03-09 PHASE4

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