Ketorolac hemicalcium
Based on 1 publication(s) in Google Scholar
Ketorolac (RS37619) hemicalcium is a non-steroidal anti-inflammatory drug (NSAID), acting as a nonselective COX inhibitor, with IC50s of 20 nM for COX-1 and 120 nM for COX-2. Ketorolac tromethamine is used as 0.5% ophthalmic solution for the research of allergic conjunctivitis, cystoid macular edema, intraoperative miosis, and postoperative ocular inflammation and pain. Ketorola chemicalcium is also a DDX3 inhibitor that can be used for cancer research.
For research use only. We do not sell to patients.
- Purity: 98.06%
- CAS No.: 167105-81-9
- Formula: C15H12CaNO3+
- Molecular Weight:274.31
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Storage:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) Ketorolac hemicalcium
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Biological Activity
Ketorolac (RS37619) salt (0-30 μM; 48 h) effectively kills the oral cancer cells[4].
Ketorolac salt (0-5 μM; 48 h) inhibits the expression of DDX3 protein, and induces apoptosis in H357 cells[4].
Ketorolac salt (0-2.5 μM; 0-16 h) inhibits the proliferation of oral cancer cells[4].
Ketorolac salt (0-50 μM) directly interacts with DDX3 and inhibits the ATPase activity[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HOK, SCC4, SCC9 and H357 cells
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Concentration:0-30 μM
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Incubation Time:48 h
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Result:Showed inhibition with IC50s of 2.6, 7.1 and 8.1 μM against H357, SCC4 and SCC9 cells, respectively. And the normal HOK cell line did not show any cell death effect.
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Cell Line:H357
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Concentration:0.5, 1.0, 1.5, 2.0 and 2.5 μM
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Incubation Time:0, 8 and 16 h
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Result:Inhibited the proliferation.
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Cell Line:H357
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Concentration:1, 2.5 and 5 μM
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Incubation Time:48 h
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Result:Significantly reduced DDX3 protein expression levels, but not completely ablated as compared to DMSO treated cells. Up regulated the expression of E-cadherin.
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Cell Line:H357
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Concentration:2.5 and 5 μM
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Incubation Time:48 h
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Result:Induced apoptosis.
Ketorolac (4 mg/kg/day, p.o.; 2 weeks) has no detrimental effect in the volume fraction of bone trabeculae formed inside the alveolar socket in rats[2].
Ketorolac (60 μg; intrathecal injection; once) attenuates the damage caused by spinal cord ischemia in rats[3].
Ketorolac salt (20 and 30 mg/kg; i.p.; two times in a week for 3 weeks) reduces oral carcinogenesis in mice[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:New Zealand White rabbits (2.0–2.7 kg), LPS endotoxin-induced ocular inflammation[1]
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Dosage:50 μL ketorolac tromethamine ophthalmic solution 0.4%
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Administration:In eyes, twice, 2 hours and 1 hour before LPS challenge
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Result:Resulted in a nearly complete inhibition (98.7%) of LPS endotoxin-induced increases in FITC (fluorescein isothiocyanate)-dextran in the anterior chamber, and resulted in a nearly complete inhibition (97.5%) of LPS endotoxin-induced increases in aqueous PGE2 concentrations in the aqueous humor.
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Animal Model:Male Wistar rats (400–450 g), spinal cord ischemia model[3]
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Dosage:30 and 60 μg
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Administration:Intrathecal injection, 1 h before the ischemia induction for once
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Result:Significantly reduced the motor disturbances and improved the survival rate at 60 μg.
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Animal Model:BALB/c mice, oral carcinogenesis model[4]
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Dosage:20 mg/kg and 30 mg/kg
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Administration:IP injection, two times in a week for 3 weeks
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Result:Decreased tumor burden, reduced expression of DDX3 and anti-apoptotic proteins (Bcl-2 and Mcl-1).
Chemical Information
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CAS No. 167105-81-9
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Appearance Solid
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Molecular Weight 274.31
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Formula C15H12CaNO3+
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Color White to off-white
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SMILES
O=C(C1C2=CC=C(C(C3=CC=CC=C3)=O)N2CC1)[O-].[Ca+2].[0.5]
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Synonyms
RS37619 hemicalcium
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Publications (1)
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Journal Impact Factor
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Most Recent
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BMC Anesthesiol
Inflammation and macrophage infiltration exacerbate adult incision response by early life injury. [Abstract]2025 Apr 10;25(1):165. PMID: 40211125
Solvent & Solubility
DMSO : 14.29 mg/mL (52.09 mM; ultrasonic and adjust pH to 3 with 1 M HCl and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Purity & Documentation
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Data Sheet (288 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
[1]. Waterbury LD, et al. Comparison of cyclooxygenase inhibitory activity and ocular anti-inflammatory effects of ketorolac tromethamine and bromfenac sodium. Curr Med Res Opin. 2006 Jun;22(6):1133-40. [Content Brief]
[2]. Fracon RN, et al. Treatment with paracetamol, ketorolac or etoricoxib did not hinder alveolar bone healing: a histometric study in rats. J Appl Oral Sci. 2010 Dec;18(6):630-4. [Content Brief]
[3]. Hsieh YC, et al. Intrathecal ketorolac pretreatment reduced spinal cord ischemic injury in rats. Anesth Analg. 2005 Apr;100(4):1134-9. [Content Brief]
[4]. Samal SK, et al. Ketorolac salt is a newly discovered DDX3 inhibitor to treat oral cancer. Sci Rep. 2015 Apr 28;5:9982. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.6455 mL | 18.2276 mL | 36.4551 mL | 91.1378 mL |
| 5 mM | 0.7291 mL | 3.6455 mL | 7.2910 mL | 18.2276 mL | |
| 10 mM | 0.3646 mL | 1.8228 mL | 3.6455 mL | 9.1138 mL | |
| 15 mM | 0.2430 mL | 1.2152 mL | 2.4303 mL | 6.0759 mL | |
| 20 mM | 0.1823 mL | 0.9114 mL | 1.8228 mL | 4.5569 mL | |
| 25 mM | 0.1458 mL | 0.7291 mL | 1.4582 mL | 3.6455 mL | |
| 30 mM | 0.1215 mL | 0.6076 mL | 1.2152 mL | 3.0379 mL | |
| 40 mM | 0.0911 mL | 0.4557 mL | 0.9114 mL | 2.2784 mL | |
| 50 mM | 0.0729 mL | 0.3646 mL | 0.7291 mL | 1.8228 mL |