Zaltoprofen - CAS 74711-43-6
Catalog number: 74711-43-6
Category: Inhibitor
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Molecular Formula:
Molecular Weight:
Cox-2 | COX
An inhibitor of Cox-1 and Cox-2;A nonsteroidal anti-inflammatory drug
Brife Description:
An inhibitor of Cox-1 and Cox-2;A nonsteroidal anti-inflammatory drug
Off-White to pale yellow crystalline solid.
10,11-dihydro-alpha-methyl-10-oxodibenzo(b,f)thiepin-2-acetic acid; Zaltoprofen; CN 100; CN-100; CN100; WY-21743; WY 21743; WY21743
DMSO 60 mg/mL (201.09 mM);Ethanol 31 mg/mL (103.9 mM)
3 years -20°C powder;6 months-80°C in solvent
Quality Standard:
Melting Point:
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1.Clinical efficacy of 0.1% pranoprofen in treatment of dry eye patients: a multicenter, randomized, controlled clinical trial.
Chen J1, Dong F1, Chen W2, Sun X3, Deng Y4, Hong J5, Zhang M6, Yang W1, Liu Z7, Xie L8. Chin Med J (Engl). 2014;127(13):2407-12.
BACKGROUND: Dry eye is a multifactorial disease of the tears and the ocular surface. This study aimed to investigate the clinical efficacy of a non-steroidal anti-inflammatory drug, pranoprofen, in the treatment of dry eye.
2.Oleic Acid Coated Gelatin Nanoparticles Impregnated Gel for Sustained Delivery of Zaltoprofen: Formulation and Textural Characterization.
Pawar S1, Pande V2. Adv Pharm Bull. 2015 Nov;5(4):537-48. doi: 10.15171/apb.2015.073. Epub 2015 Nov 30.
PURPOSE: In the present study, we have formulated zaltoprofen loaded, surface decorated, biodegradable gelatin nanogel and evaluated its texture characterization.
3.Effect of topical nonsteroidal anti-inflammatory drugs and nuclear hardness on maintenance of mydriasis during phacoemulsification surgery.
Liu C1, Liu Y, Ye S, Liu L, Zhang W, Wu M. J Ocul Pharmacol Ther. 2014 Dec;30(10):831-6. doi: 10.1089/jop.2013.0244.
PURPOSE: To compare the effects of topical nonsteroidal anti-inflammatory drugs on pupil dilation maintenance during phacoemulsification cataract surgery and quantify the relationships between pupil size change and nuclear hardness.
4.Design of nanosuspensions and freeze-dried PLGA nanoparticles as a novel approach for ophthalmic delivery of pranoprofen.
Abrego G1, Alvarado HL, Egea MA, Gonzalez-Mira E, Calpena AC, Garcia ML. J Pharm Sci. 2014 Oct;103(10):3153-64. doi: 10.1002/jps.24101. Epub 2014 Aug 4.
Pranoprofen (PF)-loaded poly (lactic-co-glycolic) acid (PLGA) nanoparticles (NPs) were optimized and characterized as a means of exploring novel formulations to improve the biopharmaceutical profile of this drug. These systems were prepared using the solvent displacement technique, with polyvinyl alcohol (PVA) as a stabilizer. A factorial design was applied to study the influence of several factors (the pH of the aqueous phase and the stabilizer, polymer and drug concentrations) on the physicochemical properties of the NPs. After optimization, the study was performed at two different aqueous phase pH values (4.50 and 5.50), two concentrations of PF (1.00 and 1.50 mg/mL), three of PVA (5, 10, and 25 mg/mL), and two of PLGA (9.00 and 9.50 mg/mL). These conditions produced NPs of a size appropriate particle size for ocular administration (around 350 nm) and high entrapment efficiency (80%). To improve their stability, the optimized NPs were lyophilized.
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CAS 74711-43-6 Zaltoprofen

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