IBUPROFEN SODIUM SALT
- CAS No.31121-93-4
- Chemical Name:IBUPROFEN SODIUM SALT
- CBNumber:CB0116983
- Molecular Formula:C13H17NaO2
- Formula Weight:228.26
- MOL File:31121-93-4.mol
- Melting point 110-112 °C
- storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
- solubility H2O: 100 mg/mL, may be clear to slightly hazy
- form Solid
- color White to Off-White
- Water Solubility H2O: 100mg/mL, clear to slightly hazy
- Stability Stable. Incompatible with strong oxidizing agents
- CAS DataBase Reference 31121-93-4
- EWG's Food Scores 1
- FDA UNII O0PJ4UZ01U
- UNSPSC Code 41116107
- NACRES NA.24
- Safety Statements :22-24/25
- WGK Germany :3
- RTECS :MU6641000
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H319-H302-H335
- Precautionary statements P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
- Brand: Sigma-Aldrich(India)
- Product number: I1892
- Product name : Ibuprofen sodium salt
- Purity: analytical standard, ≥98% (GC)
- Packaging: 100G
- Price: ₹17677.23
- Updated: 2022/06/14
- Buy: Buy
- Brand: Sigma-Aldrich(India)
- Product number: I1892
- Product name : Ibuprofen sodium salt
- Purity: analytical standard, ≥98% (GC)
- Packaging: 500G
- Price: ₹62752.53
- Updated: 2022/06/14
- Buy: Buy
IBUPROFEN SODIUM SALT Chemical Properties,Usage,Production
- Chemical Properties white powder
- Uses Ibuprofen ((±)-Ibuprofen) sodium is an orally active, selective COX-1 inhibitor with an IC50 value of 13 μM. Ibuprofen sodium inhibits cell proliferation, angiogenesis, and induces cell apoptosis. Ibuprofen sodium is a nonsteroidal anti-inflammatory agent and a nitric oxide (NO) donor. Ibuprofen sodium can be used in the research of pain, swelling, inflammation, infection, immunology, cancers[1][2][5][8].
- Application Ibuprofen sodium salt is a useful research chemical.
- Biological Activity Cyclooxygenase (COX) inhibitor th at has greater activity against COX-1 than against COX-2.
-
in vivo
Ibuprofen sodium (fed in animal feedings, 300 mg/kg, 14 days) reduces overall tumor growth and enhances anti-tumor immune characteristics without adverse autoimmune reactions in a model of postpartum breast cancer[5].
Ibuprofen sodium (subcutaneous injection, 60 mg/kg, every second day for 15 days) reduces the risk of neuropathy in a rat model of chronic Oxaliplatin?induced peripheral neuropathy[6].
Ibuprofen sodium (oral administration, 20 mg/kg, every 12 hours, 5 doses total) decreases muscle growth (average muscle fiber cross-sectional area) without affecting regulation of supraspinatus tendon adaptions to exercise[7].
Ibuprofen sodium (oral administration, 35 mg/kg, twice daily) attenuates the Inflammatory response to pseudomonas aeruginosa in a rat model of chronic pulmonary infection[8].Animal Model: Syngeneic (D2A1) orthotopic Balb/c mouse model of PPBC (postpartum)[5] Dosage: 300 mg/kg, daily for 14 days Administration: Fed in animal feedings (added to pulverized standard chow and mixed dry, then mixed with water, made into chow pellets and dried thoroughly) Result: Suppresed tumor growth, reduced presence of immature monocytes and increased numbers of T cells.
Enhanced Th1 associated cytokines as well as promoted tumor border accumulation of T cells.Animal Model: Oxaliplatin?induced peripheral neuropathy[6] Dosage: 60 mg/kg, every second day for 15 days Administration: Subcutaneous injection Result: Lowered sensory nerve conduction velocity (SNCV). - IC 50 COX-1: 13 μM (IC50); COX-2: 370 μM (IC50)
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References
[1] Noreen Y, et al. Development of a radiochemical cyclooxygenase-1 and -2 in vitro assay for identification of natural products as inhibitors of prostaglandin biosynthesis. J Nat Prod. 1998 Jan;61(1):2-7. DOI:10.1021/np970343j
[2] Hassan Akrami, et al. Inhibitory effect of ibuprofen on tumor survival and angiogenesis in gastric cancer cell. Tumour Biol. 2015 May;36(5):3237-43. DOI:10.1007/s13277-014-2952-3
[3] Sharon M Rymut, et al. Ibuprofen regulation of microtubule dynamics in cystic fibrosis epithelial cells. Am J Physiol Lung Cell Mol Physiol. 2016 Aug 1;311(2):L317-27. DOI:10.1152/ajplung.00126.2016
[4] Emmanuelle Bignon, et al. Ibuprofen and ketoprofen potentiate UVA-induced cell death by a photosensitization process. Sci Rep. 2017 Aug 21;7(1):8885. DOI:10.1038/s41598-017-09406-8
[5] Nathan D Pennock, et al. Ibuprofen supports macrophage differentiation, T cell recruitment, and tumor suppression in a model of postpartum breast cancer. J Immunother Cancer. 2018 Oct 1;6(1):98. DOI:10.1186/s40425-018-0406-y
[6] Thomas Kr?ig?rd, et al. Protective effect of ibuprofen in a rat model of chronic oxaliplatin-induced peripheral neuropathy. Exp Brain Res. 2019 Oct;237(10):2645-2651. DOI:10.1007/s00221-019-05615-x
[7] Sarah Ilkhanipour Rooney, et al. Ibuprofen Differentially Affects Supraspinatus Muscle and Tendon Adaptations to Exercise in a Rat Model. Am J Sports Med. 2016 Sep;44(9):2237-45. DOI:10.1177/0363546516646377
[8] M W Konstan, et al. Ibuprofen attenuates the inflammatory response to Pseudomonas aeruginosa in a rat model of chronic pulmonary infection. Implications for antiinflammatory therapy in cystic fibrosis. Am Rev Respir Dis. 1990 Jan;141(1):186-92. DOI:10.1164/ajrccm/141.1.186
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- L-Arginine acetylsalicylate Diclofenac sodium 4-Propylphenylacetic acid 2-(4-Methylphenyl)propanoic acid IBUPROFEN SODIUM SALT Sodium phenylacetate IBUFENAC Loxoprofen sodium 2-(4-isobutylphenyl)propionaldehyde Ibuprofen 4-Methylphenylacetic acid Phenylacetic acid (2RS)-2-(4-N-PROPYLPHENYL)PROPANOIC ACID 2-(4-ethylphenyl)acetic acid (4-ethylphenyl)acetaldehyde (2RS)-2-(4-ISOBUTYLPHENYL)PROPAN-1-OL (2RS)-2-(4-ETHYLPHENYL)PROPANOIC ACID
- 抑制剂
- 医药原料药
- 原料药
- 医药原料药-科研原料
- Analytical Standards
- Alphabetic
- Analytical Chromatography Product Catalog
- C13H17NaO2
- C13H17O2Na
- C13H18O2Na
- 二水合布洛芬钠
- 化合物 IBUPROFEN SODIUM
- 2-(4-异丁基苯基)丙酸钠
- 布洛芬钠
- 布洛芬 钠盐
- 苯乙酸, A-甲基-4-(2-甲基丙基)-,钠盐
- 31121-93-4
- (±)-Ibuprofen-d3 (sodium salt)
- sodium,2-[4-(2-methylpropyl)phenyl]propanoate
- (+/-)-Ibuprofen-d3, Sodium Salt (a-methyl-d3)
- Benzeneacetic acid, a-Methyl-4-(2-Methylpropyl)-,sodiuM salt
- Sodium ibuprofen
- Hydratropic acid, p-isobutyl-, sodium salt
- Einecs 250-477-6
- Benzeneacetic acid, alpha-methyl-4-(2-methylpropyl)-, sodium salt (9ci)
- 2-(p-Isobutylphenyl)propionic acid sodium salt
- 2-(4-Isobutylphenyl)propionic acid sodium salt
- sodiuM 2-(4-isobutylphenyl)propanoate
- (±)-Ibuprofen-d3, SodiuM Salt
- α-methyl-4-(isobutyl)phenylacetic acid
- sodium 2-(4-isobutylphenyl)propionate
- p-isobutyl-hydratropicacisodiumsalt
- ALPHA-METHYL-4-(ISOBUTYL)PHENYLACETIC ACID SODIUM SALT
- ALPHA-METHYL-4-[2-METHYLPROPYL]BENZENEACETIC ACID SODIUM SALT
- p-isobutylhydratropicacidsodiumsalt
- ibuprofensodium
- alpha-methyl-4-(2-methylpropyl)-benzeneaceticacisodiumsalt
- IBUPROFEN SODIUM SALT