MedKoo Cat#: 318182 | Name: Meloxicam
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Meloxicam is a non-steroidal anti-inflammatory agent and has been reported to inhibit the inducible isoform of Cox-2. Studies suggest that Meloxicam is Cox-2 preferential, therefore it will probably not display a lower gastrointestinal toxicity than non-selective anti-inflammatory agents. This compound has been shown to also inhibit prostanoid synthesis in inflammatory cells. It shows potent anti-inflammatory, antipyretic, and analgesic effects with low gastrointestinal toxicity in animal models.

Chemical Structure

Meloxicam
Meloxicam
CAS#71125-38-7

Theoretical Analysis

MedKoo Cat#: 318182

Name: Meloxicam

CAS#: 71125-38-7

Chemical Formula: C14H13N3O4S2

Exact Mass: 351.0348

Molecular Weight: 351.40

Elemental Analysis: C, 47.85; H, 3.73; N, 11.96; O, 18.21; S, 18.25

Price and Availability

Size Price Availability Quantity
1g USD 250.00 2 weeks
5g USD 450.00 2 weeks
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Synonym
Meloxicam; Mobic; Mobicox; Movalis; Meloxicamum; Uticox; Parocin; reumoxicam; Movicox;
IUPAC/Chemical Name
(E)-3-(hydroxy((5-methylthiazol-2-yl)amino)methylene)-2-methyl-2H-benzo[e][1,2]thiazin-4(3H)-one 1,1-dioxide
InChi Key
DWMREKMVXIFPFM-ACCUITESSA-N
InChi Code
InChI=1S/C14H13N3O4S2/c1-8-7-15-14(22-8)16-13(19)11-12(18)9-5-3-4-6-10(9)23(20,21)17(11)2/h3-7,19H,1-2H3,(H,15,16)/b13-11+
SMILES Code
CC1=CN=C(S1)NC(=O)C2=C(C3=CC=CC=C3S(=O)(=O)N2C)O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO, not in water
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Product Data
Biological target:
Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 µM and 36.6 µM for COX-2 and COX-1, respectively.
In vitro activity:
In the current study, the in vitro effects of low-dose meloxicam (0.25 µg/ml) on CF41.Mg canine mammary carcinoma cells were evaluated. Cell migration and invasion were significantly reduced following treatment with meloxicam. These results indicate that 0.25 µg/ml meloxicam reduces cell migration and invasion, in part through modulating MMP-2 and β-catenin expression. Reference: Oncol Lett. 2017 Aug;14(2):2198-2206.
In vivo activity:
In a 2-period cross-over study, synovitis was induced at T = 0 h in the L or R intercarpal joint of 6 horses by intraarticular injection of 0.5 ng lipopolysaccharide (LPS). Horses received once daily meloxicam (0.6 mg/kg bwt per os) or placebo starting at post injection hour (PIH) 2, and clinical evaluations as well as blood and synovial fluid (SF) sampling were performed at PIH 0, 8, 24 and 168. Meloxicam caused a significant reduction in lameness at PIH 8 and 24 and tended to reduce effusion. In addition, meloxicam significantly suppressed SF prostaglandin E2 and substance P release at PIH 8 and bradykinin at PIH 24 compared to placebo treatment. Reference: Equine Vet J. 2009 Sep;41(7):693-9. https://pubmed.ncbi.nlm.nih.gov/19927589/
Solvent mg/mL mM
Solubility
DMF 20.0 56.92
DMSO 33.3 94.86
DMSO:PBS (pH 7.2) (1:1) 0.5 1.42
Water 0.7 1.91
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 351.40 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
1. Iturriaga MP, Paredes R, Arias JI, Torres CG. Meloxicam decreases the migration and invasion of CF41.Mg canine mammary carcinoma cells. Oncol Lett. 2017 Aug;14(2):2198-2206. doi: 10.3892/ol.2017.6400. Epub 2017 Jun 16. PMID: 28781660; PMCID: PMC5530185. 2. Naruse T, Nishida Y, Hosono K, Ishiguro N. Meloxicam inhibits osteosarcoma growth, invasiveness and metastasis by COX-2-dependent and independent routes. Carcinogenesis. 2006 Mar;27(3):584-92. doi: 10.1093/carcin/bgi240. Epub 2005 Oct 11. PMID: 16219634. 3. de Grauw JC, van de Lest CH, Brama PA, Rambags BP, van Weeren PR. In vivo effects of meloxicam on inflammatory mediators, MMP activity and cartilage biomarkers in equine joints with acute synovitis. Equine Vet J. 2009 Sep;41(7):693-9. doi: 10.2746/042516409x436286. PMID: 19927589. 4. Jones CJ, Streppa HK, Harmon BG, Budsberg SC. In vivo effects of meloxicam and aspirin on blood, gastric mucosal, and synovial fluid prostanoid synthesis in dogs. Am J Vet Res. 2002 Nov;63(11):1527-31. doi: 10.2460/ajvr.2002.63.1527. PMID: 12428662.
In vitro protocol:
1. Iturriaga MP, Paredes R, Arias JI, Torres CG. Meloxicam decreases the migration and invasion of CF41.Mg canine mammary carcinoma cells. Oncol Lett. 2017 Aug;14(2):2198-2206. doi: 10.3892/ol.2017.6400. Epub 2017 Jun 16. PMID: 28781660; PMCID: PMC5530185. 2. Naruse T, Nishida Y, Hosono K, Ishiguro N. Meloxicam inhibits osteosarcoma growth, invasiveness and metastasis by COX-2-dependent and independent routes. Carcinogenesis. 2006 Mar;27(3):584-92. doi: 10.1093/carcin/bgi240. Epub 2005 Oct 11. PMID: 16219634.
In vivo protocol:
1. de Grauw JC, van de Lest CH, Brama PA, Rambags BP, van Weeren PR. In vivo effects of meloxicam on inflammatory mediators, MMP activity and cartilage biomarkers in equine joints with acute synovitis. Equine Vet J. 2009 Sep;41(7):693-9. doi: 10.2746/042516409x436286. PMID: 19927589. 2. Jones CJ, Streppa HK, Harmon BG, Budsberg SC. In vivo effects of meloxicam and aspirin on blood, gastric mucosal, and synovial fluid prostanoid synthesis in dogs. Am J Vet Res. 2002 Nov;63(11):1527-31. doi: 10.2460/ajvr.2002.63.1527. PMID: 12428662.
1: Low-dose meloxicam (Vivlodex) for osteoarthritis pain. Med Lett Drugs Ther. 2016 Mar 14;58(1490):35-6. PubMed PMID: 26963155. 2: Almukainzi M, Jamali F, Aghazadeh-Habashi A, Löbenberg R. Disease specific modeling: Simulation of the pharmacokinetics of meloxicam and ibuprofen in disease state vs. healthy conditions. Eur J Pharm Biopharm. 2016 Mar;100:77-84. doi: 10.1016/j.ejpb.2015.12.004. Epub 2016 Jan 2. PubMed PMID: 26752427. 3: Alomrani AH, Badran MM. Flexosomes for transdermal delivery of meloxicam: characterization and antiinflammatory activity. Artif Cells Nanomed Biotechnol. 2016 Feb 28:1-8. [Epub ahead of print] PubMed PMID: 26924417. 4: Takami Y, Eguchi S, Tateishi M, Ryu T, Mikagi K, Wada Y, Saitsu H. A randomised controlled trial of meloxicam, a Cox-2 inhibitor, to prevent hepatocellular carcinoma recurrence after initial curative treatment. Hepatol Int. 2016 Feb 4. [Epub ahead of print] PubMed PMID: 26846471. 5: Ianiski FR, Alves CB, Ferreira CF, Rech VC, Savegnago L, Wilhelm EA, Luchese C. Meloxicam-loaded nanocapsules as an alternative to improve memory decline in an Alzheimer's disease model in mice: involvement of Na(+), K(+)-ATPase. Metab Brain Dis. 2016 Feb 27. [Epub ahead of print] PubMed PMID: 26922073.