Recent Advances in the Synthesis and Pharmacological Evaluation of Naproxen Derivatives: A Review.
Naproxen is a medication classified as a non-steroidal Anti-Inflammatory Drug (NSAIDs) utilized for its anti-inflammatory properties. The principal functional group in naproxen is the carboxyl group, prompting numerous researchers to modify this group to synthesize novel derivatives of naproxen and...
| Publicado en: | Journal of Advances in Medical & Biomedical Research Vol. 33; pp. 13 - 31 |
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| Autores principales: | , , |
| Formato: | pictorial review tables/charts Journal Article |
| Publicado: |
Zanjan University of Medical Sciences & Health Services
2025 Special Issue
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=191904520&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 191904520 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 26766264 N5MJ jtl: Journal of Advances in Medical & Biomedical Research issn: 26766264 maglogo: N pubinfo: dt: 2025 Special Issue vid: 33 pid: 65276 pub: Zanjan University of Medical Sciences & Health Services artinfo: ui: 191904520 191904520 191904520 10.30699/jambr.33.162.13 191904520 ppf: 13 ppct: 18 formats: fmt: @attributes: type: P tig: atl: Recent Advances in the Synthesis and Pharmacological Evaluation of Naproxen Derivatives: A Review. aug: au: Al-Musawi, Ahmed J. Mashaf, Abdulateef Abdulkadhim Amran, Mohammed affil: Department of Chemistry, College of Science, University of Misan, Maysan, 62001, Iraq. sug: subj: Naproxen Analogs and Derivatives Drug Design Methods Molecular Structure Antiinflammatory Agents, Non-Steroidal Pharmacodynamics Chemistry, Organic Methods Antiinflammatory Agents Pharmacodynamics Cox-2 Inhibitors Pharmacodynamics Analgesics, Nonnarcotic Pharmacodynamics Antineoplastic Agents Pharmacodynamics Drug Toxicity Carboxylic Acids Drug Efficacy Prostatic Neoplasms Drug Therapy Heterocyclic Compounds Thiazoles Pharmacodynamics Amines Pharmacodynamics Amino Acids Pharmacodynamics Patient Safety Chemical Phenomena ab: Naproxen is a medication classified as a non-steroidal Anti-Inflammatory Drug (NSAIDs) utilized for its anti-inflammatory properties. The principal functional group in naproxen is the carboxyl group, prompting numerous researchers to modify this group to synthesize novel derivatives of naproxen and investigate their pharmacological efficacy, to discover more effective molecules than naproxen. This review examines the methodologies for synthesizing derivatives, with an emphasis on notable molecules exhibiting unique biological activity and the key techniques employed in these investigations. Modification involves introducing a triazole 5n moiety via transformation of the carboxyl group which has been found to enhance the efficacy of the derivative and constitute a potential treatment for prostate cancer. Some pyrazole and pyrazoline derivatives have shown anti-inflammatory and antiproliferative activity, like derivative 9c which demonstrated high antioxidant activity due to the presence of a methoxy group (an electron-donating group), which increased its potency. It also exhibited vigorous anti-proliferative activity against MCF-7 cells, with an IC50 value of 1.49 μM. Research has also found that modifying the carboxyl group of naproxen to derivatives containing sulfur-containing heterocyclic rings, such as thiazole and thiadiazole 14a and 22q, whether as single or fused rings, enhances its anti-inflammatory and analgesic activity. Amines and amino acids 26a, 26b, 29b, 32b, and 33b have also been observed to enhance their anti-inflammatory and analgesic activity. These compounds exhibited high oral absorption and were not carcinogenic or toxic in rodent studies, showing safety and minimal ulceration. The most prominent derivatives that inhibit the Cyclooxygenase-2 (COX-2) enzyme are hydrazone derivatives that contain the functional group (-NH-N=CH-), and the substituted m-chlorophenyl 35c emerged as the most inhibitory derivative. Structural modification at the carboxyl group of naproxen yields diverse derivatives with enhanced pharmacological profiles and potential safety advantages over the parent compound. pubtype: Academic Journal doctype: pictorial review tables/charts Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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